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- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion type Assertion NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_head.
- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion description "[Seventeen unrelated families with RP and an apparent X-linked pattern of disease inheritance were identified from the Swedish RP registry and screened for mutations in the RP2 and RPGR (for the RP3 disease) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_provenance.
- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion evidence source_evidence_literature NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_provenance.
- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion SIO_000772 14566651 NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_provenance.
- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion wasDerivedFrom befree-20140225 NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_provenance.
- NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_assertion wasGeneratedBy ECO_0000203 NP675410.RAMiogIq5ZEnLxWPfXzeziUlkVyXle59wl70RKybDfoLM130_provenance.