Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_assertion wasGeneratedBy ECO_0000203 NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_assertion wasDerivedFrom lhgdn-20090331 NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_assertion SIO_000772 12783933 NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_assertion evidence source_evidence_literature NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_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." NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.