Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_assertion description "[The majority of associated anomalies, with the exception of psychomotor retardation and Chiari malformation, were detected more frequently in TWIST1 patients than in FGFR3 p.P250R patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_assertion evidence source_evidence_literature NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_assertion SIO_000772 22544111 NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_assertion wasDerivedFrom befree-20140225 NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_assertion wasGeneratedBy ECO_0000203 NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846929.RAcK2sW08QUpyyuWdv7UYaTINOrvxLzh9FxBDn2XyPNrQ130_provenance.