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- source_evidence_literature type ECO_0000212 NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- befree-2016 importedOn "2016-02-19" NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_assertion wasGeneratedBy ECO_0000203 NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_assertion wasDerivedFrom befree-2016 NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_assertion SIO_000772 16015425 NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_assertion evidence source_evidence_literature NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.
- NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_assertion description "[A patient with hemophilia A is reported who had an acute myocardial infarction and in whom investigation for hereditary thrombophilia showed a prothrombotic molecular defect, the G20210A prothrombin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503978.RAnfutnoGsaVxB3hLiyrhliNzdKTvhjDKB9XQJh-leyLM130_provenance.