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- source_evidence_literature type ECO_0000212 NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_assertion description "[Herein are illustrated some pitfalls in the diagnosis of melanoma, as well as variants of Spitz's nevus that correlate with specific genomic aberrations such as gains of chromosome 11p and loss of the BAP-1 gene on chromosome 3p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_assertion evidence source_evidence_literature NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_assertion SIO_000772 22648325 NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_assertion wasDerivedFrom befree-20150227 NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_assertion wasGeneratedBy ECO_0000203 NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673174.RAn5GJZk7YX_4eCFqsyZ4WQdgfQDcKFFSrC1cpv1Oxl3o130_provenance.