Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_assertion wasGeneratedBy ECO_0000203 NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_assertion wasDerivedFrom befree-20150227 NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_assertion SIO_000772 19500772 NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_assertion evidence source_evidence_literature NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.
- NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_assertion description "[In contrast to the association of point mutations in FOXF1 with bowel malrotation, microdeletions of FOXF1 were associated with hypoplastic left heart syndrome and gastrointestinal atresias, probably due to haploinsufficiency for the neighboring FOXC2 and FOXL1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404739.RA0haxrGQk4EbHeQkgIAdZa8MxCj4sV42BRUY92qxNWbI130_provenance.