Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_assertion wasGeneratedBy ECO_0000203 NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_assertion wasDerivedFrom befree-20150227 NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_assertion SIO_000772 23076529 NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_assertion evidence source_evidence_literature NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.
- NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_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." NP918287.RAQbtk714p27WOlWmzHpWWbVdRFAzVUaxGVxHBR6Ayfiw130_provenance.