Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_assertion description "[This study emphasises the principal role of ABCC6 mutations in the pathogenesis of PXE, but the reasons for phenotypic variability remain to be explored.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_assertion evidence source_evidence_literature NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_assertion SIO_000772 17617515 NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_assertion wasDerivedFrom gad-20130706 NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_assertion wasGeneratedBy ECO_0000203 NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP59591.RAXzp02XLaWHYCkrmeCJ-cn2bAkaA7oYMBQugn85xchRk130_provenance.