Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- befree-2016 importedOn "2016-02-19" NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_assertion wasGeneratedBy ECO_0000203 NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_assertion wasDerivedFrom befree-2016 NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_assertion SIO_000772 17347910 NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_assertion evidence source_evidence_literature NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.
- NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_assertion description "[In our study, diagnosis of FH and related disorders (ApoB-100 defect) by means of conventional laboratory methods missed at least 21% in children and 42% in adults affected with LDLR and/or ApoB gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598007.RAuTZgTDylu8Hzi71AKwrDUFqoHPr8WZhAZVDc79x9ki0130_provenance.