Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion> ?p ?o ?g. }
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- NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion type Assertion NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_head.
- NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion description "[Mutations in the PCSK9 gene are associated with variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_provenance.
- NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion evidence source_evidence_literature NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_provenance.
- NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion SIO_000772 16211558 NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_provenance.
- NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion wasDerivedFrom lhgdn-20090331 NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_provenance.
- NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_assertion wasGeneratedBy ECO_0000203 NP134766.RAYXeHK_HnWQIHYl108uL2TXZ8Jv0PTyz15fvkuJ3mJDU130_provenance.