Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion> ?p ?o ?g. }
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- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion type Assertion NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_head.
- 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.