Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_assertion wasGeneratedBy ECO_0000203 NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_assertion wasDerivedFrom befree-20150227 NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_assertion SIO_000772 12783933 NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_assertion evidence source_evidence_literature NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.
- NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_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." NP789858.RAJkn2N02MXDyECceg0YCKLNZB7pLhHw-bIt-sgEBAFEw130_provenance.