Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP676637.RA1bB9kqf52QLjFSVCmQv44o1m4CqgCYzE4T_e_Asw9AI130_provenance.