Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion type Assertion NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_head.
- NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion description "[Frequencies and distributions of NAT2 and UGT1A7 SNPs as well as their haplotypes were investigated in 95 patients with UC, 60 patients with CD, and 200 gender-matched, unrelated, healthy, control volunteers by PCR-restriction fragment length polymorphism (RFLP), PCR-denaturing high-performance liquid chromatography (DHPLC), and direct DNA sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_provenance.
- NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion evidence source_evidence_literature NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_provenance.
- NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion SIO_000772 16097053 NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_provenance.
- NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion wasDerivedFrom befree-20140225 NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_provenance.
- NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_assertion wasGeneratedBy ECO_0000203 NP468015.RAk-EoLZg7Ws70Qh5K0MoT8DE81NnAhsxY67JV5nZkclQ130_provenance.