Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_assertion type Assertion NP204513.RAdy8lWkVcnRihyW-xsvPqIqjiag-rZYfEHkOgQx7CHYI130_head.
- 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.