Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_assertion type Assertion NP945807.RArChfKnTwRt0fMOEdawIPfMFX4Y31cx2M784PG4fWn2Q130_head.
- 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.