Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_assertion description "[The insertion-deletion (I/D) polymorphism of the angiotensin converting enzyme gene is a diallelic polymorphism that constitutes a genetic influence on the progression of renal diseases such as IgA nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_assertion evidence source_evidence_literature NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_assertion SIO_000772 10099885 NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_assertion wasDerivedFrom befree-2016 NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_assertion wasGeneratedBy ECO_0000203 NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.
- befree-2016 importedOn "2016-02-19" NP248889.RA18T1n63G_YWdCuXjjF7qHeQdAZDLJPpI9c_QCyHEsUo130_provenance.