Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion wasGeneratedBy ECO_0000203 NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion wasDerivedFrom befree-20140225 NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion SIO_000772 23076529 NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion evidence source_evidence_literature NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion description "[There is evidence suggesting that genetic variants of Nodal signaling may be associated with risk of congenital heart diseases (CHDs), in which several polymorphisms, such as Nodal rs1904589, have been considered to be implicated in the accumulation of the genetic burden of CHD risk with interacting genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance.