Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_assertion description "[We then screened 200 T2D siblings/families for PSMD9 +nt460A/G, +nt437C/T and exon E197G A/G single nucleotide polymorphisms (SNPs) and performed a non-parametric linkage study to test for linkage for coronary artery disease, stroke/TIA, macro-vasculopathy and macrovascular pathology of T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_assertion evidence source_evidence_literature NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_assertion SIO_000772 21496327 NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_assertion wasDerivedFrom befree-20150227 NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_assertion wasGeneratedBy ECO_0000203 NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP652192.RASSQSEkdEVLFCbSrXs-xLV9tUgC3CDbzfNtsdQTuHYR0130_provenance.