Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion> ?p ?o ?g. }
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- NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_assertion type Assertion NP453298.RAyq6dUjfrGuyxK22EWp2nd04jhRL8wsfOeGNQ0ZQHhA4130_head.
- 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.