Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_assertion description "[In about a decade, mutations in 8 different genes (IPF1, EIF2AK3, GK, FOXP3, KCNJ11, ABCC8, PTF1A and GLIS3) have been discovered in patients with the permanent form of the disease, and 3 genetic abnormalities (defects in the paternally imprinted chromosomal region 6q24 and 'mild' activating mutations in KCNJ11 or ABCC8) have been detected in subjects with transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_assertion evidence source_evidence_literature NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_assertion SIO_000772 17986829 NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_assertion wasDerivedFrom befree-2016 NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_assertion wasGeneratedBy ECO_0000203 NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.
- befree-2016 importedOn "2016-02-19" NP639142.RAANmhDq_XtQ4N-iKsaFKYPCoNvJiD8ok9DdI4Dy_XH14130_provenance.