Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion type Assertion NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_head.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion description "[Our results support the following conclusions: (i) somatic mutation of the CDKN2 gene is rare in sporadic melanomas with allelic loss at 9p21; (ii) homozygous loss is more frequent than mutation of the CDKN2 gene in sporadic melanomas; (iii) at 9p21-p23 genes other than CDKN2 may be involved in the development of sporadic melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion evidence source_evidence_literature NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion SIO_000772 8631588 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion wasDerivedFrom befree-20140225 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.
- NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_assertion wasGeneratedBy ECO_0000203 NP756068.RA8X1T9lKzv7c2XVpheJRHyGrWKnjVPsngokX1Fmeu0dk130_provenance.