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- NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_assertion type Assertion NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_head.
- NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_assertion wasGeneratedBy ECO_0000203 NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_provenance.
- NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_assertion wasDerivedFrom lhgdn-20090331 NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_provenance.
- NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_assertion SIO_000772 15146389 NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_provenance.
- NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_assertion evidence source_evidence_literature NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_provenance.
- NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_assertion description "[Missense Mutation in HOXD10 is associated with congenital vertical talus and Charcot-Marie-Tooth disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205017.RAWbStmEgsvbjTlfpd_AaoGYtCn8ncqzcd0zEfLzWP8NU130_provenance.