Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_assertion description "[Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_assertion evidence source_evidence_literature NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_assertion SIO_000772 20384727 NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_assertion wasDerivedFrom befree-20140225 NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_assertion wasGeneratedBy ECO_0000203 NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP293433.RAPBaBOfsOKGafht3QIIkdWmW5YJz6D4dppRzmqtt1dW0130_provenance.