Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_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." NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_assertion evidence source_evidence_literature NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_assertion SIO_000772 21515823 NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_assertion wasDerivedFrom befree-20150227 NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_assertion wasGeneratedBy ECO_0000203 NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP415598.RAkRRpQUuPIyheWpPdKfhbg5ULSMr0wYNK6Vw93iyqwG8130_provenance.