Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion> ?p ?o ?g. }
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- NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion type Assertion NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_head.
- NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion description "[We set out to measure the frequency of sequence variants in PAK3 in schizophrenia without premorbid MR. We conducted complete gene reseqeuncing of all coding exons and exon-intron boundaries in patients with schizophrenia with cognitive impairment but without premorbid MR. Deleterious variants in schizophrenia alone were rare (<1/159 or 0.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion evidence source_evidence_literature NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion SIO_000772 18805672 NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion wasDerivedFrom befree-2016 NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_assertion wasGeneratedBy ECO_0000203 NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.