Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_assertion wasGeneratedBy ECO_0000203 NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_assertion wasDerivedFrom befree-20140225 NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_assertion SIO_000772 12838518 NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_assertion evidence source_evidence_literature NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_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." NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_provenance.