Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion> ?p ?o ?g. }
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- NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion type Assertion NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_head.
- NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion wasGeneratedBy ECO_0000218 NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_provenance.
- NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion wasDerivedFrom ctd_human-2016 NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_provenance.
- NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion SIO_000772 12730697 NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_provenance.
- NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion evidence source_evidence_curated NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_provenance.
- NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_assertion description "[Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP12900.RARL8yo-eWhfLVsYXFvQqL16T4OpEhiRXjnlydlziSSIU130_provenance.