Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_assertion> ?p ?o ?g. }
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- NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_assertion type Assertion NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_head.
- NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_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." NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_provenance.
- NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_assertion evidence source_evidence_literature NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_provenance.
- NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_assertion SIO_000772 18805967 NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_provenance.
- NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_assertion wasDerivedFrom befree-20140225 NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_provenance.
- NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_assertion wasGeneratedBy ECO_0000203 NP766458.RAgCcnTN3Y4WIz12BzRqqcL-6ui9XuHoH0rs-nBEaENkk130_provenance.