Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_assertion description "[EEC syndrome type 3 with a heterozygous germline mutation in the P63 gene and B cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_assertion evidence source_evidence_literature NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_assertion SIO_000772 12838557 NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_assertion wasDerivedFrom befree-20150227 NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_assertion wasGeneratedBy ECO_0000203 NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP799601.RA16mYQmvm8Gc2vQCbcY5mJMwLaj3jNVq6vWxI1_fCPdg130_provenance.