Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion> ?p ?o ?g. }
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- NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion type Assertion NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_head.
- NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion description "[To investigate if single nucleotide polymorphisms on chromosome 12p13 and within 11 kb of the gene NINJ2 would be associated with earlier-onset (vs. late-onset) first-ever ischemic stroke and increase silent cerebrovascular lesions prior to the manifestation of the stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_provenance.
- NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion evidence source_evidence_literature NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_provenance.
- NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion SIO_000772 22429733 NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_provenance.
- NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion wasDerivedFrom befree-20150227 NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_provenance.
- NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_assertion wasGeneratedBy ECO_0000203 NP591729.RAHO4NtsD0vsNhyeaVMWEAld4vEfM6NmVdeRrQfCUUagA130_provenance.