Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_assertion evidence source_evidence_literature NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_assertion SIO_000772 16453125 NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_assertion wasDerivedFrom befree-20140225 NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_assertion wasGeneratedBy ECO_0000203 NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP735833.RACOBEJe5TFO9UjoF4qH0kbaif3z8MpV18jMsuwLubgvg130_provenance.