Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion> ?p ?o ?g. }
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- NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion type Assertion NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_head.
- NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion description "[Missense variants in the BRCA2 gene are routinely detected during clinical screening for pathogenic mutations in patients with a family history of breast and ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_provenance.
- NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion evidence source_evidence_literature NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_provenance.
- NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion SIO_000772 24323938 NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_provenance.
- NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion wasDerivedFrom befree-2016 NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_provenance.
- NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_assertion wasGeneratedBy ECO_0000203 NP1135342.RAAwXtT3YVBK3JSHOM7vjXinWZDOD-LCv6iCUUu-t8MnM130_provenance.