Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_assertion description "[SLC2A2 mutations are an autosomal recessive cause of neonatal diabetes that should be considered in consanguineous families or those with TNDM, after excluding common causes, even in the absence of features of FBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_assertion evidence source_evidence_literature NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_assertion SIO_000772 22660720 NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_assertion wasDerivedFrom befree-20150227 NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_assertion wasGeneratedBy ECO_0000203 NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP696114.RApdZuCHxKcNXZcK1MbzAAqZfp7eF1KoZIToU71UrODY8130_provenance.