Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_assertion description "[Genome-wide association analysis of the FHS data detected two new gene regions with genome-wide significance, detected epistatic SNP effects on TC and HDL-C with the significance of suggestive linkage in seven pairs of gene regions, and confirmed some previously reported gene regions associated with TC and HDL-C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_assertion evidence source_evidence_literature NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_assertion SIO_000772 20370913 NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_assertion wasDerivedFrom gad-20130706 NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_assertion wasGeneratedBy ECO_0000203 NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP75587.RAN2ReD1j2c8V_ohu9JEzkHGGyEyBaFSF_h4Q7vLsFSEM130_provenance.