Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion> ?p ?o ?g. }
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- NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion type Assertion NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_head.
- NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion description "[Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_provenance.
- NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion evidence source_evidence_curated NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_provenance.
- NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion SIO_000772 20890276 NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_provenance.
- NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion wasDerivedFrom ctd_human-20150221 NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_provenance.
- NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_assertion wasGeneratedBy ECO_0000218 NP16339.RARwaUUhRb7umATlLQDys1iuUnLu6oRTDV_vDc1Fais2k130_provenance.