Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion> ?p ?o ?g. }
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- NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion type Assertion NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_head.
- NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion description "[To further our clinical understanding of familial BC and examine whether haematological malignancies are predictive of ATM germline mutation, we estimated the frequency of heterozygote mutation carriers in a series of 122 BC women with a family history of both BC and haematological malignancy and without BRCA1/2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_provenance.
- NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion evidence source_evidence_literature NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_provenance.
- NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion SIO_000772 19404735 NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_provenance.
- NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion wasDerivedFrom befree-20140225 NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_provenance.
- NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_assertion wasGeneratedBy ECO_0000203 NP211929.RAsjzFByVFqNheV0bEjj05PeymqtM9qyI-aRQNBu080l4130_provenance.