Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_assertion description "[To investigate the role of the TDP-43 gene in sporadic forms of frontotemporal dementia (FTD), we genotyped 10 single nucleotide polymorphisms covering the entire TDP-43 genomic region, including the MASP2 gene in 173 patients with sporadic FTD (including 7 patients that were diagnosed with FTD and ALS) and 184 matched controls from Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_assertion evidence source_evidence_literature NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_assertion SIO_000772 17614162 NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_assertion wasDerivedFrom befree-20140225 NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_assertion wasGeneratedBy ECO_0000203 NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP618577.RAdILprRevrSLKftYTz86e1zv1alVgAAB1Z-yEJf4FOsQ130_provenance.