Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_assertion evidence source_evidence_literature NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_assertion SIO_000772 16648378 NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_assertion wasDerivedFrom befree-2016 NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_assertion wasGeneratedBy ECO_0000203 NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.
- befree-2016 importedOn "2016-02-19" NP547526.RAb83SPU8y2s8uRcKhIQBIdv-RAI2XaSGfQ3w8WOBbl0g130_provenance.