Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_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." NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_assertion evidence source_evidence_literature NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_assertion SIO_000772 19160128 NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_assertion wasDerivedFrom befree-20140225 NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_assertion wasGeneratedBy ECO_0000203 NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506358.RAUu6vTGMO5JbWQ0y_1wadmaClS8o5H_2Shmoxnw4QvNA130_provenance.