Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_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." NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_assertion evidence source_evidence_literature NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_assertion SIO_000772 18805672 NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_assertion wasDerivedFrom befree-20150227 NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_assertion wasGeneratedBy ECO_0000203 NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP608273.RAadZ3zdmuOcBBWeXkIDEXZxyGV1CqYAEp3GD8toIIfcU130_provenance.