Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_assertion> ?p ?o ?g. }
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- NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_assertion type Assertion NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_head.
- NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_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." NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_provenance.
- NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_assertion evidence source_evidence_literature NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_provenance.
- NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_assertion SIO_000772 18553546 NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_provenance.
- NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_assertion wasDerivedFrom befree-2016 NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_provenance.
- NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_assertion wasGeneratedBy ECO_0000203 NP676645.RAITs_tDgCd8h9aeFLoJQm0rwkFKP2TitX9377PGR7A-Y130_provenance.