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- source_evidence_literature type ECO_0000212 NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_assertion description "[However, HFE mutations were seen twice as often among carriers of a common BRCA2 mutation 9346(-2)A-->G compared with the rest of the MBC cases, indicating that HFE may be an MBC risk modifier gene among BRCA2 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_assertion evidence source_evidence_literature NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_assertion SIO_000772 16003728 NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_assertion wasDerivedFrom befree-2016 NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_assertion wasGeneratedBy ECO_0000203 NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.
- befree-2016 importedOn "2016-02-19" NP503025.RAluWl7N8fp1LQ5Faj0_n69M0nfKQWgivN294WdFFe_og130_provenance.