Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_assertion description "[Mutations in the genes encoding for low-density lipoprotein receptor (LDLR), apolipoprotein B (APOB), and proprotein convertase subtilisin/kexin 9 (PCSK9) underlie ADH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_assertion evidence source_evidence_literature NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_assertion SIO_000772 21382890 NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_assertion wasDerivedFrom befree-2016 NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_assertion wasGeneratedBy ECO_0000203 NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.
- befree-2016 importedOn "2016-02-19" NP877671.RAObcQKMS0HCvo4DGDd6EWZJ5qUAJ8203gE6afJamhVVI130_provenance.