Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion type Assertion NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_head.
- NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion wasGeneratedBy ECO_0000203 NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_provenance.
- NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion wasDerivedFrom befree-2016 NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_provenance.
- NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion SIO_000772 17262179 NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_provenance.
- NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion evidence source_evidence_literature NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_provenance.
- NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_assertion description "[We would like to highlight the fact that 14.3% of patients with 3 or more cases of breast cancer in the family, and 16.7% of patients with family history of breast and ovarian cancer, present a pathological mutation in BRCA1 or BRCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591327.RAn9ilndTdd7AQVzna2EfH9A3o21XaPetrHNAnduwVGyI130_provenance.