Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_assertion> ?p ?o ?g. }
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- NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_assertion type Assertion NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_head.
- NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_assertion wasGeneratedBy ECO_0000203 NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_provenance.
- NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_assertion wasDerivedFrom lhgdn-20090331 NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_provenance.
- NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_assertion SIO_000772 12783933 NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_provenance.
- NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_assertion evidence source_evidence_literature NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_provenance.
- NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_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." NP181733.RAI3yl7Av04dO48QuuN1DV3S-HrY6ADq7hX4DL0S5trRA130_provenance.