http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#head http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#provenance http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://rdf.disgenet.org/resource/gda/DGNe39235bd5478348dc85ef9412811db16 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2149 http://rdf.disgenet.org/resource/gda/DGNe39235bd5478348dc85ef9412811db16 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0032897 http://rdf.disgenet.org/resource/gda/DGNe39235bd5478348dc85ef9412811db16 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001123 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#provenance http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://purl.org/dc/terms/description [One PWS subject with maternal disomy 15 showed weak but detectable expression of PAR1, whereas SNRPN expression was detected in two PWS subjects [one with the 15q11-q13 deletion and one with a t(15;15) karyotype and maternal disomy 15], and the remaining typical PWS subjects showed no expression of the imprinted genes or transcripts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/11258349 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/dc/terms/created 2017-10-17T13:12:35+02:00 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP377236.RAJQ7iyz-vSv_NxR7wAZt9u_Y8ZRFAZL7X9whb5s9FFJE http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0