Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- befree-2016 importedOn "2016-02-19" NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_assertion wasGeneratedBy ECO_0000203 NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_assertion wasDerivedFrom befree-2016 NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_assertion SIO_000772 12783933 NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_assertion evidence source_evidence_literature NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.
- NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_assertion description "[Activating mutations in NRAS codon 61, all of which were either CAA(Gln)-AAA(Lys) or CAA(Gln)-CGA(Arg) mutations, were found in 95% (20/21) of primary hereditary melanomas but in only 10% (1/10) of sporadic melanomas (P<.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396719.RAhHVOyzwoqHqkKak0y48EmHCG2C2D4PbZ_gqfdsWtebk130_provenance.