Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_assertion description "[Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_assertion evidence source_evidence_curated NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_assertion SIO_000772 23222558 NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_assertion wasDerivedFrom uniprot-2016 NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_assertion wasGeneratedBy ECO_0000218 NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7287.RAXuNg6PunhTwzURFXEI6vOGdTbzUOW4Ex7EVPz60LJFc130_provenance.