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- source_evidence_literature type ECO_0000212 NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion description "[This review article will discuss (1) the BRCA1 and BRCA2 genes within the larger context of homologous recombination deficiency; (2) the advances in our understanding of hereditary cancer risk and the dramatic shifts that have occurred in the genetic testing landscape since the landmark 2013 Supreme Court ruling invalidating patents on BRCA1 and BRCA2 genetic testing; and (3) the clinical trials leading to the approval of olaparib, the first in human PARP inhibitor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion evidence source_evidence_literature NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion SIO_000772 25725131 NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion wasDerivedFrom befree-2016 NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_assertion wasGeneratedBy ECO_0000203 NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266984.RAs1FAs8hSLMpTB4jFxgW_Nh8j9SI-ngoqAS0rGho1IhY130_provenance.