Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion> ?p ?o ?g. }
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- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion type Assertion NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_head.
- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion description "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_provenance.
- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion evidence source_evidence_literature NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_provenance.
- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion SIO_000772 11810296 NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_provenance.
- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion wasDerivedFrom befree-2016 NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_provenance.
- NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_assertion wasGeneratedBy ECO_0000203 NP343262.RAaHt3dDcZttKbR8p29Sfn-nahDp_4klrHsPuiPiZ7HC0130_provenance.