Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion wasGeneratedBy ECO_0000203 NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion wasDerivedFrom lhgdn-20090331 NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion SIO_000772 12783933 NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion evidence source_evidence_literature NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion description "[high frequency of NRAS codon 61 mutations detected in primary hereditary melanomas may be the result of a hypermutability phenotype associated with a hereditary predisposition for melanoma development in patients with germline CDKN2A mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.