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- source_evidence_literature type ECO_0000212 NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_assertion description "[Multiplex XLMR pedigrees have been reported with only one mutated patient having autism and MR: different X-located MR genes have been shown to be involved (NLGN4, MECP2, OPHN1, ZNF674 and FRAXA) which does not suggest that they could be 'autism genes'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_assertion evidence source_evidence_literature NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_assertion SIO_000772 19160128 NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_assertion wasDerivedFrom befree-20150227 NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_assertion wasGeneratedBy ECO_0000203 NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP354729.RAQKBSHa1o3q-dmLcgE4Vko9YRJqHv6CsjWWB974h50Kc130_provenance.