Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_assertion description "[To test genetic variation associated with treatment related VTE in patient peripheral blood DNA, we used a custom-built molecular inversion probe (MIP)-based single nucleotide polymorphism (SNP) chip containing 3404 SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_assertion evidence source_evidence_literature NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_assertion SIO_000772 18805967 NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_assertion wasDerivedFrom befree-20140225 NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_assertion wasGeneratedBy ECO_0000203 NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP698971.RACfXG9Th9VF8UEXZgaSTL1MxVoZuu2VSGo9MGHHwOsPE130_provenance.