Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_assertion> ?p ?o ?g. }
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- NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_assertion type Assertion NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_head.
- NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_assertion wasGeneratedBy ECO_0000203 NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_provenance.
- NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_assertion wasDerivedFrom befree-2016 NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_provenance.
- NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_assertion SIO_000772 11851376 NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_provenance.
- NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_assertion evidence source_evidence_literature NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_provenance.
- NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_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." NP345571.RA83dufFwCqSVv3hWe4PUKGRT7DVqiKXYWw1_04oT-WH0130_provenance.