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- source_evidence_literature type ECO_0000212 NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_assertion description "[Today, more than 60 mutations in the factor XIIIA- and B-subunit genes are known leading to congenital factor XIII deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_assertion evidence source_evidence_literature NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_assertion SIO_000772 16543965 NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_assertion wasDerivedFrom befree-2016 NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_assertion wasGeneratedBy ECO_0000203 NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.
- befree-2016 importedOn "2016-02-19" NP540808.RAex9b453-C4tLByqLqvb88QSVZNdGz5nqZNWhL--ub40130_provenance.