Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_assertion type Assertion NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_head.
- NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_assertion wasGeneratedBy ECO_0000203 NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_provenance.
- NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_assertion wasDerivedFrom befree-20150227 NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_provenance.
- NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_assertion SIO_000772 11851376 NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_provenance.
- NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_assertion evidence source_evidence_literature NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_provenance.
- NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_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." NP533638.RADc7zyf5Zz3dvKWYsnorZdG5Okr1gXqnwPq-yvpjcHBc130_provenance.