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- source_evidence_literature type ECO_0000212 NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_assertion description "[A large number of rare sequence variants of unknown clinical significance have been identified in the breast cancer susceptibility genes, BRCA1 and BRCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_assertion evidence source_evidence_literature NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_assertion SIO_000772 20174566 NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_assertion wasDerivedFrom befree-2016 NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_assertion wasGeneratedBy ECO_0000203 NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.
- befree-2016 importedOn "2016-02-19" NP795076.RAAsBxVZfcCR3i8xnm3Vxn7JeRWMLW4SrJgbNJs9Otc3w130_provenance.