Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_assertion wasGeneratedBy ECO_0000203 NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_assertion wasDerivedFrom befree-20140225 NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_assertion SIO_000772 17347910 NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_assertion evidence source_evidence_literature NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_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." NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208657.RAi08Y29VZg5wcbmFWdM1ggqsCzoId2l-I5r5CC4Xssg8130_provenance.