Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion> ?p ?o ?g. }
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- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion type Assertion NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_head.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion wasGeneratedBy ECO_0000203 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion wasDerivedFrom befree-20140225 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion SIO_000772 11851376 NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion evidence source_evidence_literature NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.
- NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_assertion description "[DNA samples of 98 unrelated Belgian patients with a family history of autosomal dominant hypercholesterolaemia were screened for mutations in the LDLR gene, after exclusion of known mutations causing familial defective apolipoprotein B-100 (FDB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755528.RADSv9CZDXk04upTuqZCmQ8vYTPheZ_UMF_JwJ3PMWcqU130_provenance.