Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_assertion description "[Three mutations of CFTR were detected in four ACP patients with a prevalence (8.9%) not significantly different from that observed (3.0%) in ALD patients and from that expected (3.2%) in our geographical area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_assertion evidence source_evidence_literature NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_assertion SIO_000772 12939655 NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_assertion wasDerivedFrom befree-20140225 NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_assertion wasGeneratedBy ECO_0000203 NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453561.RAwkoFVlEiKoq4P0Qd3L7vxMrSyyFQ1H6Aimjrxskzu6o130_provenance.