Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- befree-2016 importedOn "2016-02-19" NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_assertion wasGeneratedBy ECO_0000203 NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_assertion wasDerivedFrom befree-2016 NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_assertion SIO_000772 18162506 NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_assertion evidence source_evidence_literature NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.
- NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_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." NP647318.RAD_XCEz1670Q8iari5wUvvUOrJXsCdwWfLpG-VRPt5rA130_provenance.