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- source_evidence_literature type ECO_0000212 NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_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.
- 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.
- befree-2016 importedOn "2016-02-19" NP1081019.RA1Xa0oJQTFLaVHvfS7KA6ycBR85bnh48T-9PsU0VLW5Q130_provenance.