Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
- befree-2016 importedOn "2016-02-19" NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
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- NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_assertion wasDerivedFrom befree-2016 NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
- NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_assertion SIO_000772 12838518 NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
- NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_assertion evidence source_evidence_literature NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.
- NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_assertion description "[Missense DCX mutations may manifest as non-syndromic mental retardation with cryptogenic epilepsy in female subjects and SBH in boys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400202.RAI13tJtoG5owpy7XmKyQV6-HEXeXPJ-M0ubbRuvfX1QI130_provenance.