Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP694168.RAFdOrce5ajn6HJGpfa6VAMuPT-gK5mfZG7o6RGcYtGu0130_provenance.