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- NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_assertion type Assertion NP349808.RAanTQFIGzvsbDZ6JG2ZLjlwCIQQGxrFxHm-rc1KlOk0U130_head.
- 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.