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- NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_assertion type Assertion NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_head.
- NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_assertion wasGeneratedBy ECO_0000218 NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_provenance.
- NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_assertion wasDerivedFrom uniprot-2016 NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_provenance.
- NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_assertion SIO_000772 9741700 NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_provenance.
- NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_assertion evidence source_evidence_curated NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_provenance.
- NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_assertion description "[Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9871.RAG2t4sQqaK7MtVtCgsP1delwrLkx-lJkHdpq_fHFsb8I130_provenance.