Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion> ?p ?o ?g. }
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- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion type Assertion NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_head.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion evidence source_evidence_literature NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion SIO_000772 22833210 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion wasDerivedFrom befree-2016 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion wasGeneratedBy ECO_0000203 NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.