Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- befree-2016 importedOn "2016-02-19" NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_assertion wasGeneratedBy ECO_0000203 NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_assertion wasDerivedFrom befree-2016 NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_assertion SIO_000772 15530918 NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_assertion evidence source_evidence_literature NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.
- NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_assertion description "[No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467767.RAaaGKUKlJyar6Oo-dckYRETe2e6WqFmchDLDOh1XngPE130_provenance.