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- source_evidence_literature type ECO_0000212 NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_assertion description "[To determine the criteria that may be used to select patients for BRCA treatment-focused genetic testing, we performed a systemic literature search of studies that assessed BRCA1 and BRCA2 mutation frequency in women with ovarian cancer unselected for family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_assertion evidence source_evidence_literature NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_assertion SIO_000772 20973257 NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_assertion wasDerivedFrom befree-2016 NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_assertion wasGeneratedBy ECO_0000203 NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.
- befree-2016 importedOn "2016-02-19" NP847831.RAX6h6q-sA3WEkX1uzcuVuCdm549S6iChBvySXLEEbtvY130_provenance.