Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_assertion wasGeneratedBy ECO_0000203 NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_assertion wasDerivedFrom befree-20150227 NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_assertion SIO_000772 8045710 NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_assertion evidence source_evidence_literature NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.
- NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760956.RAl3T2ndrJ75Wd-vM2M_JKwUn4VUZecJ4NTmPGAkLOboI130_provenance.