Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_assertion description "[We have tested the effect of NRN1 sequence variation on susceptibility to SZ and on general cognitive ability in patients and non-psychiatric control subjects by re-sequencing the coding regions of NRN1 and its flanking sequences, and genotyping 19 single-nucleotide polymorphisms (SNPs) in 336 SZ patients and 172 healthy control individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_assertion evidence source_evidence_literature NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_assertion SIO_000772 19569075 NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_assertion wasDerivedFrom befree-20150227 NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_assertion wasGeneratedBy ECO_0000203 NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP904133.RA39S5hyo-oMMBrKNnLkUb5SC_sQPWtejt7ZGvpa-wBnM130_provenance.