Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion> ?p ?o ?g. }
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- NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion type Assertion NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_head.
- NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion description "[Among patients with melanoma genetically tested, CDKN2A G101W mutation carriers were more frequently younger (P�=�0.023), with clinically atypical nevi (P�=�0.050), with cytological atypia (P�=�0.033) at confocal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.
- NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion evidence source_evidence_literature NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.
- NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion SIO_000772 23711066 NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.
- NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion wasDerivedFrom befree-2016 NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.
- NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_assertion wasGeneratedBy ECO_0000203 NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.