Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion> ?p ?o ?g. }
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- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion type Assertion NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_head.
- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion wasGeneratedBy ECO_0000203 NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_provenance.
- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion wasDerivedFrom gad-20150221 NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_provenance.
- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion SIO_000772 20353281 NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_provenance.
- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion evidence source_evidence_literature NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_provenance.
- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_provenance.