Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_assertion description "[We screened for novel genomic variants of LRP1/A2MR and investigated the importance of these variants in 214 coronary patients suffering from myocardial infarction as well as in 224 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_assertion evidence source_evidence_literature NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_assertion SIO_000772 12402342 NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_assertion wasDerivedFrom befree-2016 NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_assertion wasGeneratedBy ECO_0000203 NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP372598.RA9FCmdQWnj3-XSw9qVefevnopL0MXfs6Jz-YZLv6qoCQ130_provenance.