Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion> ?p ?o ?g. }
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- NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion type Assertion NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_head.
- NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion wasGeneratedBy ECO_0000203 NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_provenance.
- NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion wasDerivedFrom befree-20150227 NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_provenance.
- NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion SIO_000772 12783933 NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_provenance.
- NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion evidence source_evidence_literature NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_provenance.
- NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_assertion description "[Activating mutations in NRAS codon 61, all of which were either CAA(Gln)-AAA(Lys) or CAA(Gln)-CGA(Arg) mutations, were found in 95% (20/21) of primary hereditary melanomas but in only 10% (1/10) of sporadic melanomas (P<.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014354.RATfjwi1ApccutS0RtzzVx5ZoK_CQ_7wiDGvC3i9ne2kE130_provenance.