Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_assertion description "[In conclusion, our study reveals a novel cellular phenotype in recessive NDI in that AQP2-P262L acts as a mutant in dominant NDI, except for that its missorting is overruled by apical sorting of wt-AQP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_assertion evidence source_evidence_literature NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_assertion SIO_000772 15509592 NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_assertion wasDerivedFrom befree-2016 NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_assertion wasGeneratedBy ECO_0000203 NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.
- befree-2016 importedOn "2016-02-19" NP466388.RAGQHrban15_0fUOFGkFX04OgMi8PdU7UG0QaE8_Fmjps130_provenance.