Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_assertion wasGeneratedBy ECO_0000218 NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_assertion wasDerivedFrom uniprot-2016 NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_assertion SIO_000772 18162506 NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_assertion evidence source_evidence_curated NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.
- NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_assertion description "[Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5218.RAF1IpXQShBJ3uod62Ym30s0XTM9UhaY-z90uSW1Ks-ds130_provenance.