Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP527111.RAzqEnSZbU7W2vfm11-JU9pLsT79pu2z1Z0HjsxbQLULU130_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." NP527111.RAzqEnSZbU7W2vfm11-JU9pLsT79pu2z1Z0HjsxbQLULU130_provenance.
- NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_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." NP305462.RA0f5uw8uguE-1VUvIkfBLC7jZidrDlYPKSnSoaJP5SWo130_provenance.
- 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.