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- source_evidence_literature type ECO_0000212 NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_assertion description "[Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_assertion evidence source_evidence_literature NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_assertion SIO_000772 25186627 NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_assertion wasDerivedFrom befree-2016 NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_assertion wasGeneratedBy ECO_0000203 NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216595.RAvKHaFtjG67FhS4vVYhXr72-icb-vHkra8Pvn4Ek-Ano130_provenance.