Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_assertion description "[This survey underlines the allelic heterogeneity of ABCA1 mutations and suggests that: (i) TD subjects, if asymptomatic, may be overlooked and (ii) there may be a selection bias in genotyping towards carriers of ABCA1 mutations who have pCAD possibly related to a combination of genetic and environmental cardiovascular risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_assertion evidence source_evidence_curated NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_assertion SIO_000772 15019541 NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_assertion wasDerivedFrom uniprot-2016 NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_assertion wasGeneratedBy ECO_0000218 NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3319.RAige1_32-Gl_VcE3GzIzz2qoSl6O1D2h5l7klKrlFI0c130_provenance.