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- source_evidence_literature type ECO_0000212 NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_assertion description "[In conclusion, our results indicate a minor role for the HFE mutations C282Y and H63D in the causation of MBC and PC, but carriers of both BRCA2 9346(-2)A-->G and an HFE mutation may be at an increased risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_assertion evidence source_evidence_literature NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_assertion SIO_000772 16003728 NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_assertion wasDerivedFrom befree-2016 NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_assertion wasGeneratedBy ECO_0000203 NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.
- befree-2016 importedOn "2016-02-19" NP503027.RArcYgmqMbCo4UUIw3qDak2nkSt4-WKeok_VoB4MC-4XY130_provenance.