Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_assertion wasGeneratedBy ECO_0000203 NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_assertion wasDerivedFrom befree-20150227 NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_assertion SIO_000772 12783933 NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_assertion evidence source_evidence_literature NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.
- NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_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." NP246855.RA3XA0DzyA42kcOjub4vqbSzU_1GJ2o8aDoXco3EHHRQQ130_provenance.