Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion wasGeneratedBy ECO_0000203 NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion wasDerivedFrom befree-20140225 NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion SIO_000772 19896112 NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion evidence source_evidence_literature NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion description "[Heterozygous copy-number variants and SNPs of CNTNAP2 and NRXN1, two distantly related members of the neurexin superfamily, have been repeatedly associated with a wide spectrum of neuropsychiatric disorders, such as developmental language disorders, autism spectrum disorders, epilepsy, and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_provenance.