Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion description "[No germline mutations were detected in the VHL or MET genes, suggesting that FCRC is not allelic with VHL disease or HPRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion evidence source_evidence_literature NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion SIO_000772 10807693 NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion wasDerivedFrom befree-20150227 NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion wasGeneratedBy ECO_0000203 NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_provenance.