Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion type Assertion NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_head.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_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." NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_provenance.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion evidence source_evidence_literature NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_provenance.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion SIO_000772 18805672 NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_provenance.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion wasDerivedFrom befree-20140225 NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_provenance.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion wasGeneratedBy ECO_0000203 NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_provenance.