Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion> ?p ?o ?g. }
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- NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion type Assertion NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_head.
- NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion description "[To verify the accuracy of proposed genetic modifiers influencing stroke risk in SCA, we performed genotyping for 38 published single nucleotide polymorphisms (SNPs), as well as ?-thalassemia, G6PD A(-) variant deficiency, and ?-globin haplotype in 2 cohorts of children with well-defined stroke phenotypes (130 stroke, 103 nonstroke).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_provenance.
- NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion evidence source_evidence_literature NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_provenance.
- NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion SIO_000772 21515823 NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_provenance.
- NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion wasDerivedFrom befree-2016 NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_provenance.
- NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_assertion wasGeneratedBy ECO_0000203 NP889242.RAQLJFW7v9H3s6FjsK9YWVXw27yltLkPmrcBucwEzlCHU130_provenance.