http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#head
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#assertion
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#provenance
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#assertion
http://rdf.disgenet.org/resource/gda/DGN6f9d9b08c27c45959b722f5e7834d604
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1822
http://rdf.disgenet.org/resource/gda/DGN6f9d9b08c27c45959b722f5e7834d604
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0020179
http://rdf.disgenet.org/resource/gda/DGN6f9d9b08c27c45959b722f5e7834d604
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#provenance
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#assertion
http://purl.org/dc/terms/description
[The study on 244 patients referred with the clinical diagnosis of HD and without mutation of the IT15 gene revealed one case of SCA17 but did not disclose the presence of two other diseases with a similar clinical manifestation: DRPLA and HDL2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#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/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18651325
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/GAD
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/GAD
http://purl.org/pav/importedOn
2017-02-21
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/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/dc/terms/created
2017-10-17T13:12:06+02:00
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP302043.RAvefzlQl6cyw9757k5qaDlr_E50fQT3QDMNRKm5AUoOs
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