Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion description "[The use of data on genetic variants and the addition of data on global monocytic gene expression led to the identification of the novel functional CAD susceptibility locus LIPA, located on chromosome 10q23.31. The respective eSNPs associated with CAD strongly affect LIPA gene expression level, which was related to endothelial dysfunction, a precursor of CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion evidence source_evidence_literature NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion SIO_000772 21606135 NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion wasDerivedFrom gad-20130706 NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion wasGeneratedBy ECO_0000203 NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance.