Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_assertion description "[A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_assertion evidence source_evidence_curated NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_assertion SIO_000772 16613899 NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_assertion wasDerivedFrom uniprot-20130724 NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_assertion wasGeneratedBy ECO_0000218 NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP89.RAvan4uS2KKRJKj2RA4pF9UzjL6UATviydZkCt0VA__2k130_provenance.