Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_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." NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_assertion evidence source_evidence_literature NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_assertion SIO_000772 22429733 NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_assertion wasDerivedFrom befree-2016 NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_assertion wasGeneratedBy ECO_0000203 NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.
- befree-2016 importedOn "2016-02-19" NP968812.RASLjIdBkhXlwIbKdAEpXvNY0TwfuLtkTzRTyQNfLsTn8130_provenance.