Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion> ?p ?o ?g. }
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- NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion type Assertion NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_head.
- NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion description "[Familial defective apolipoprotein B-100 (FDB) R3500Q is an autosomal co-dominant disorder caused by the substitution of glutamine for arginine at amino acid residue 3500 of the apolipoprotein B-100 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_provenance.
- NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion evidence source_evidence_literature NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_provenance.
- NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion SIO_000772 10795369 NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_provenance.
- NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion wasDerivedFrom befree-2016 NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_provenance.
- NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_assertion wasGeneratedBy ECO_0000203 NP282929.RADwrAFw8Z45BCISAQ62gRk9ozu2W-WwMd1f6Xd4KQuoQ130_provenance.