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- NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_assertion type Assertion NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_head.
- NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_assertion description "[We evaluated patients with hereditary retinal diseases featuring subretinal spots (retinitis punctata albescens and fundus albipunctatus) and patients with typical dominant or recessive retinitis pigmentosa for mutations in RDH5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_provenance.
- NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_assertion evidence source_evidence_literature NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_provenance.
- NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_assertion SIO_000772 10369264 NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_provenance.
- NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_assertion wasDerivedFrom befree-20140225 NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_provenance.
- NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_assertion wasGeneratedBy ECO_0000203 NP508643.RAmjLqth9DawK6xU_wCZ6D2dyiG_mWbsCVn6y7NJ-qbDg130_provenance.