Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_assertion description "[We conclude that genetic variation in the ALOX5AP gene contributes to CHD risk in patients with FH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_assertion evidence source_evidence_literature NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_assertion SIO_000772 18775537 NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_assertion wasDerivedFrom befree-20140225 NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_assertion wasGeneratedBy ECO_0000203 NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP573756.RAw-Rc14DNq-fnWEfLWqxA7Oh9xyTHoa-yxkfqwvYgSAE130_provenance.