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- source_evidence_literature type ECO_0000212 NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_assertion description "[The most common inherited traits (deficiency in antithrombin, protein C, or protein S, factor V Leiden, prothrombin G20210A) and mild hyperhomocysteinemia are diagnosed in at least 40% of patients with venous thromboembolism (VTE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_assertion evidence source_evidence_literature NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_assertion SIO_000772 12368166 NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_assertion wasDerivedFrom befree-2016 NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_assertion wasGeneratedBy ECO_0000203 NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.
- befree-2016 importedOn "2016-02-19" NP370110.RA-oWNef7uOec3ZpdsNQJud6wbQlZ9GnoCVg9_uKFp6pw130_provenance.