Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion> ?p ?o ?g. }
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- NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion type Assertion NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_head.
- NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion description "[Haplotype analysis suggest common founders in carriers of the recurrent BRCA2 mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_provenance.
- NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion evidence source_evidence_literature NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_provenance.
- NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion SIO_000772 16539696 NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_provenance.
- NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion wasDerivedFrom gad-20150221 NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_provenance.
- NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_assertion wasGeneratedBy ECO_0000203 NP99475.RAawt2MVUblbWzxRXqLTfFU-VFN2oTRK_GCDvPhY3PZAw130_provenance.