Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_assertion description "[Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_assertion evidence source_evidence_curated NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_assertion SIO_000772 10102298 NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_assertion wasDerivedFrom uniprot-2016 NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_assertion wasGeneratedBy ECO_0000218 NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP80.RAYc5LKDQL2QUIvBBlDY7z6Wz2RQxOs36OJ8ug5R2l_Cc130_provenance.