Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_assertion description "[In this study, we screened the ARX gene in 226 male patients with autism spectrum disorders and mental retardation; 42 of the patients had epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_assertion evidence source_evidence_literature NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_assertion SIO_000772 17044103 NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_assertion wasDerivedFrom befree-20150227 NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_assertion wasGeneratedBy ECO_0000203 NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978097.RA07a7g1Z2QNHNXxnRh3x1KRSWYcvlo9V9w3egt0RD4PU130_provenance.