http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#head
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#assertion
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#provenance
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#assertion
http://rdf.disgenet.org/resource/gda/DGN7edd4a5d1830ba56f4a3772b63f70272
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1822
http://rdf.disgenet.org/resource/gda/DGN7edd4a5d1830ba56f4a3772b63f70272
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0007761
http://rdf.disgenet.org/resource/gda/DGN7edd4a5d1830ba56f4a3772b63f70272
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#provenance
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#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/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#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/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18651325
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/GAD
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#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/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/dc/terms/created
2017-10-17T13:12:06+02:00
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP302486.RAnPBx_uEN51YFmDiFNG8EnzoIprxkPGBh2G91KOTC5FM
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