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- NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_assertion type Assertion NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_head.
- NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_assertion description "[These discrepancies were compounded with the finding of RPGR mutations leading exclusively to X-linked cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_provenance.
- NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_assertion evidence source_evidence_literature NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_provenance.
- NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_assertion SIO_000772 12140192 NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_provenance.
- NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_assertion wasDerivedFrom befree-20140225 NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_provenance.
- NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_assertion wasGeneratedBy ECO_0000203 NP611728.RAD_rzk2hUDsS06uWsP2Y7_eIjx_LuK5GgZ2gwExaNHCs130_provenance.