Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_assertion description "[The androgen receptor contains a polymorphic polyglutamine repeat and expansion of this repeat to beyond approximately 40 causes spinobulbar muscular atrophy (SBMA; also known as Kennedy's disease), a genetic form of motor neurone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_assertion evidence source_evidence_literature NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_assertion SIO_000772 10643885 NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_assertion wasDerivedFrom befree-20140225 NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_assertion wasGeneratedBy ECO_0000203 NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439175.RA2JRXaObKePAXkcxd5qM_UeHtM-PzSjZxLlBjHfbVLxk130_provenance.