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- source_evidence_literature type ECO_0000212 NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_assertion description "[We analyzed allelic variants of USF1 and APOA5 in families (n=516) ascertained for atherogenic dyslipidemia and in an autopsy series of middle-aged men (n=300) with precise quantitative measurements of atherosclerotic lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_assertion evidence source_evidence_literature NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_assertion SIO_000772 19910639 NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_assertion wasDerivedFrom befree-20150227 NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_assertion wasGeneratedBy ECO_0000203 NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP966283.RAXydeX6iPPtfA7JRkqOSB2NQJC4ZInKlHnea4v_3QUDE130_provenance.