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- source_evidence_literature type ECO_0000212 NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_assertion description "[NRAS mutations were the most prevalently identified additional mutations and were highly associated with malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_assertion evidence source_evidence_literature NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_assertion SIO_000772 23585181 NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_assertion wasDerivedFrom befree-20150227 NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_assertion wasGeneratedBy ECO_0000203 NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP598513.RAtc7TE_ubWzskwAvkJugufhI1P5JLbMq-RSkkuhMSMrI130_provenance.