Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_assertion wasGeneratedBy ECO_0000203 NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_assertion wasDerivedFrom befree-20140225 NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_assertion SIO_000772 12783933 NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_assertion evidence source_evidence_literature NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_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." NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP788870.RAXjquVu_TixTH8U6Aeypq-abOI_4x0AWd9wE2043_sxI130_provenance.