Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_assertion description "[The HRAS1 variable number of tandem repeats (VNTR) polymorphism, 1 kb downstream from the HRAS1 gene, has been reported to be associated with risk of various cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_assertion evidence source_evidence_literature NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_assertion SIO_000772 12115522 NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_assertion wasDerivedFrom befree-20150227 NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_assertion wasGeneratedBy ECO_0000203 NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788898.RAnzU_fiQdOciGVgrmOB1TEaYE7S2AT6a6InhchEQonko130_provenance.