Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_assertion description "[These results show that LIPH is a second causative gene for ARWH/hypotrichosis, giving rise to a phenotype clinically indistinguishable from P2RY5 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_assertion evidence source_evidence_literature NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_assertion SIO_000772 18830268 NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_assertion wasDerivedFrom befree-20140225 NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_assertion wasGeneratedBy ECO_0000203 NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435515.RA3TJSN_hJahyl5ncrktLf7M3tKFBIlyG-A1fy_BbpKOY130_provenance.