Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_assertion description "[The predominant cardiac defects in Fgfr2-IIIb mutant embryos are ventricular septal defects associated with overriding aorta or double outlet right ventricle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_assertion evidence source_evidence_literature NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_assertion SIO_000772 16687131 NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_assertion wasDerivedFrom befree-20150227 NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_assertion wasGeneratedBy ECO_0000203 NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP401811.RAA_vze0_H-fR-Dp7yR4wKH7n2NSilmT1sVQwEy5FZyLU130_provenance.