Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_assertion description "[Mouse models of XLAG, ISSX and other human ARX mutations demonstrate a direct genotype-phenotype correlation in ARX-related neurologic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_assertion evidence source_evidence_literature NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_assertion SIO_000772 24236044 NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_assertion wasDerivedFrom befree-20150227 NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_assertion wasGeneratedBy ECO_0000203 NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719303.RASLtbSGiDb7VjIVo-3PM5DxAl4RGDn3auwO9ZgI2dI0E130_provenance.