Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion description "[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion evidence source_evidence_literature NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion SIO_000772 15955369 NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion wasDerivedFrom befree-20140225 NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion wasGeneratedBy ECO_0000203 NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance.