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- NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_assertion type Assertion NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_head.
- NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_assertion description "[L1 syndrome and X-linked NDI are distinct clinical disorders caused by mutations in the L1CAM and AVPR2 genes, respectively, located in adjacent positions in Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_assertion evidence source_evidence_literature NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_assertion SIO_000772 18553546 NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_assertion wasDerivedFrom befree-2016 NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_assertion wasGeneratedBy ECO_0000203 NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.