Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_assertion description "[Either GRIN2B or GRIN2A, encoding the NMDA receptor subunits NR2B and NR2A, was found to be disrupted by chromosome translocation breakpoints in individuals with mental retardation and/or epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_assertion evidence source_evidence_literature NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_assertion SIO_000772 20890276 NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_assertion wasDerivedFrom befree-2016 NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_assertion wasGeneratedBy ECO_0000203 NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.
- befree-2016 importedOn "2016-02-19" NP843494.RA3StovkLKB7nv2QCB9yKCc78aZUrzPaEcpALcysj0hc8130_provenance.