Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_assertion> ?p ?o ?g. }
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- NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_assertion type Assertion NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_head.
- NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_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." NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_provenance.
- NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_assertion evidence source_evidence_literature NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_provenance.
- NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_assertion SIO_000772 20890276 NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_provenance.
- NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_assertion wasDerivedFrom befree-20140225 NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_provenance.
- NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_assertion wasGeneratedBy ECO_0000203 NP924782.RAWAoe_J6eVlpSKEv1iw0pduJjj22pXnAUIRW7A5rjywg130_provenance.