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- source_evidence_literature type ECO_0000212 NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_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 stro]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_assertion evidence source_evidence_literature NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_assertion SIO_000772 21606135 NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_assertion wasDerivedFrom gad-20150221 NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_assertion wasGeneratedBy ECO_0000203 NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP159452.RAqxQowRznZliIRIw5KiK3SSsb7K_lofT59wJrsm6f7hw130_provenance.