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- source_evidence_literature type ECO_0000212 NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_assertion description "[Mutations in the Aristaless-related homeobox gene, ARX, have been a cause of X-linked mental retardation (XLMR) and are responsible for a vast phenotypic spectrum including syndromic and non-syndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_assertion evidence source_evidence_literature NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_assertion SIO_000772 17613295 NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_assertion wasDerivedFrom befree-20140225 NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_assertion wasGeneratedBy ECO_0000203 NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP193446.RAYhYd6s5LVl2ZfEP174RFycu17BrqNebp6HYygjNO-vk130_provenance.