Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_assertion description "[Deficiency of ornithine-delta-aminotransferase (OAT) in humans causes hyperornithinaemia and gyrate atrophy (GA), a blinding chorioretinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_assertion evidence source_evidence_literature NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_assertion SIO_000772 7550347 NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_assertion wasDerivedFrom befree-20150227 NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_assertion wasGeneratedBy ECO_0000203 NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP601376.RAomSFNir2K88W_MFuDItPsC8q_g7O_dGLB9OfRzoPskA130_provenance.