Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion description "[These data, within the context of previous studies, clarify the risk of specific genetic variants in TNFA and therefore the role of TNF-? in the overall AP syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion evidence source_evidence_literature NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion SIO_000772 22487520 NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion wasDerivedFrom befree-20140225 NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion wasGeneratedBy ECO_0000203 NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_provenance.