http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#head
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#assertion
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#provenance
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#assertion
http://rdf.disgenet.org/resource/gda/DGNa64273e9e05443861c88ebb7e95acb2b
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/367
http://rdf.disgenet.org/resource/gda/DGNa64273e9e05443861c88ebb7e95acb2b
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0752353
http://rdf.disgenet.org/resource/gda/DGNa64273e9e05443861c88ebb7e95acb2b
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#provenance
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#assertion
http://purl.org/dc/terms/description
[This review summarizes the most recent information on two pathologies linked to mutations of the androgen receptor, namely, the complete androgen insensitivity syndrome (CAIS) and the spinal and bulbar muscular atrophy (SBMA or Kennedy's disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#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/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/16388114
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#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/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/dc/terms/created
2017-10-17T13:10:43+02:00
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP84374.RA2N_mA3CuogKCCad0CccLsghbA9GmWi3frsXF1MzNlMY
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