Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion type Assertion NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_head.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion wasGeneratedBy ECO_0000203 NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_provenance.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion wasDerivedFrom lhgdn-20090331 NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_provenance.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion SIO_000772 12783933 NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_provenance.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion evidence source_evidence_literature NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_provenance.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_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." NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_provenance.