Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_assertion description "[Hereditary pancreatic carcinoma shows extant phenotypic and genotypic heterogeneity as evidenced by its integral association with a variety of hereditary cancer syndromes inclusive of the familial atypical multiple mole melanoma (FAMMM) syndrome in concert with CDKN2A (p16) germline mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_assertion evidence source_evidence_literature NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_assertion SIO_000772 11815963 NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_assertion wasDerivedFrom befree-20140225 NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_assertion wasGeneratedBy ECO_0000203 NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP838913.RANgvzcrsLwIlIEtY1LKRUj5RhS_Ml0CLZcjDHbQvzOtE130_provenance.