Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_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." NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_assertion evidence source_evidence_literature NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_assertion SIO_000772 19569075 NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_assertion wasDerivedFrom gad-20130706 NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_assertion wasGeneratedBy ECO_0000203 NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.
- gad-20130706 importedOn "2013-07-06" NP90360.RA6xN52vqQNNzrm7PxHme4NWCi_1G2_12f96015fXGo7Y130_provenance.