Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_assertion description "[Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_assertion evidence source_evidence_literature NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_assertion SIO_000772 16715098 NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_assertion wasDerivedFrom befree-2016 NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_assertion wasGeneratedBy ECO_0000203 NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.
- befree-2016 importedOn "2016-02-19" NP550785.RAI_jZIcLBG-tej-pdu7HI5ZR3gMFMlR_LvoLfFX6t_fs130_provenance.