Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_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." NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_assertion evidence source_evidence_literature NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_assertion SIO_000772 21515823 NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_assertion wasDerivedFrom befree-20140225 NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_assertion wasGeneratedBy ECO_0000203 NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP528408.RA5_CcokIhvIGeeISHew9RglL29HtRpPlh3SHnh6N5UFU130_provenance.