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- source_evidence_literature type ECO_0000212 NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_assertion description "[While there were no significant differences in the distribution of SELP or PSGL-1 alleles or genotypes between patients and controls, a trend for a significant association of the C-2123G genotypes distribution with incident CHD was observed (P=0.06).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_assertion evidence source_evidence_literature NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_assertion SIO_000772 20376705 NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_assertion wasDerivedFrom befree-20140225 NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_assertion wasGeneratedBy ECO_0000203 NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP734806.RAxbemDTpkjPrkrtM-tEzUKzaNERru6qaFIXvaf7EH6QQ130_provenance.