Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_assertion wasGeneratedBy ECO_0000203 NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_assertion wasDerivedFrom gad-20150221 NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_assertion SIO_000772 19319977 NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_assertion evidence source_evidence_literature NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.
- NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_assertion description "[The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143766.RAYm3tQu7NkvfHaFuIWN4ys1yJE6q5ZJ6qGqLN_V4hfoo130_provenance.