Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_assertion description "[199 multiplex families with AS with four non-synonymous single nucleotide polymorphisms (SNPs), three in the endoplasmic reticulum aminopeptidase 1 (ERAP1) gene (rs27044, rs10050860 and rs30187) and one in the endoplasmic reticulum aminopeptidase 2 (ERAP2) gene (rs2549782), were genotyped and family-based association analyses were performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_assertion evidence source_evidence_literature NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_assertion SIO_000772 19433412 NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_assertion wasDerivedFrom gad-20130706 NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_assertion wasGeneratedBy ECO_0000203 NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP70571.RAfzyXnb8ia0MvBmIcN8C9nNtvhTA8-PVcH3fqpUObqIE130_provenance.