Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_assertion description "[These results extend our previous observations and indicate that defects in XPCC cause Xeroderma pigmentosum group C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_assertion evidence source_evidence_literature NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_assertion SIO_000772 8298653 NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_assertion wasDerivedFrom befree-20140225 NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_assertion wasGeneratedBy ECO_0000203 NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP289681.RA8HdJuUOM2Cr793VUpfAhSU6oGFleyGoqLf5KVh_D76Q130_provenance.