Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_assertion description "[Mutations in the pancreatic ATP sensitive K(+) channel proteins [sulfonyluea receptor 1 (SUR1) and inward rectifier K(+) channel Kir6.2 (Kir6.2), encoded by ATP-binding cassette transporter subfamily C member 8 (ABCC8) and potassium channel J11 (KCNJ11), respectively], are the most common cause of neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_assertion evidence source_evidence_literature NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_assertion SIO_000772 22831748 NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_assertion wasDerivedFrom befree-2016 NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_assertion wasGeneratedBy ECO_0000203 NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1000181.RAMLMQ_-WFYiNqYOtWP3UK8aW1G9Tqe6uVd6SNicniOAw130_provenance.