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- source_evidence_literature type ECO_0000212 NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_assertion evidence source_evidence_literature NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_assertion SIO_000772 12215251 NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_assertion wasDerivedFrom befree-2016 NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_assertion wasGeneratedBy ECO_0000203 NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- befree-2016 importedOn "2016-02-19" NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.