Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_assertion description "[X-linked congenital stationary night blindness (CSNB) is a nonprogressive retinal disorder characterized by impaired night vision, variably involving high myopia, nystagmus, decreased visual acuity, and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_assertion evidence source_evidence_literature NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_assertion SIO_000772 10982042 NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_assertion wasDerivedFrom befree-20140225 NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_assertion wasGeneratedBy ECO_0000203 NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP461522.RA2CzsUFJN7DzY3iDKSmx-mIj5FxzcjWlukLLijoMhdxY130_provenance.