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- source_evidence_literature type ECO_0000212 NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_assertion description "[However, several genes involved in SOA have been recently identified, namely N-MYC, SOX2, and CHD7 involved in Feingold (MIM 164280), anophthalmia-oesophageal-genital (MIM 600992) and CHARGE syndromes respectively (MIM 214800), suggesting that OA/TOF, at least in their syndromic forms, may be a highly genetically heterogeneous group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_assertion evidence source_evidence_literature NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_assertion SIO_000772 17489843 NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_assertion wasDerivedFrom befree-20140225 NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_assertion wasGeneratedBy ECO_0000203 NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP686584.RAAJOgiI0I-M9DyP5M5v9uRyxfL1h_QuOGb-ALsjPEUAc130_provenance.