Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_assertion wasGeneratedBy ECO_0000218 NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_assertion wasDerivedFrom uniprot-20130724 NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_assertion SIO_000772 18162506 NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_assertion evidence source_evidence_curated NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_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." NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3268.RAevH_7YXrytlH73VvcDZj-qTyCFc-rxRNDLmUFAe73lE130_provenance.