Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_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." NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_assertion evidence source_evidence_literature NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_assertion SIO_000772 18805672 NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_assertion wasDerivedFrom befree-20140225 NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_assertion wasGeneratedBy ECO_0000203 NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.