Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion> ?p ?o ?g. }
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- NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion type Assertion NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_head.
- NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion wasGeneratedBy ECO_0000203 NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_provenance.
- NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion wasDerivedFrom befree-2016 NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_provenance.
- NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion SIO_000772 17347910 NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_provenance.
- NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion evidence source_evidence_literature NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_provenance.
- NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_assertion description "[In our study, diagnosis of FH and related disorders (ApoB-100 defect) by means of conventional laboratory methods missed at least 21% in children and 42% in adults affected with LDLR and/or ApoB gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598001.RAJeL6snZL-cF90INrERbMCTZ3ph2dyQ05cOqKF1baeqg130_provenance.