Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_assertion description "[The Tyr99Cys GUCA1A mutation has been previously shown to cause autosomal dominant progressive cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_assertion evidence source_evidence_literature NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_assertion SIO_000772 15953638 NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_assertion wasDerivedFrom befree-20150227 NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_assertion wasGeneratedBy ECO_0000203 NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP441905.RAfI0unHEL83ed_W_xPRoglXrlWz07jSMrBK8JHTrWQAY130_provenance.