Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_assertion wasGeneratedBy ECO_0000203 NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_assertion wasDerivedFrom befree-2016 NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_assertion SIO_000772 23771925 NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_assertion evidence source_evidence_literature NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.
- NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_assertion description "[Our study aims were to determine the frequency of MODY mutations (HNF1A, HNF4A, glucokinase) in a diverse population of youth with diabetes and to assess how well clinical features identify youth with maturity-onset diabetes of the young (MODY).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086449.RAwAbWwlPnnOQ34TmPwxdnaHmLD4Y70SfgXLaINwPydnU130_provenance.