Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_assertion wasGeneratedBy ECO_0000203 NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_assertion wasDerivedFrom lhgdn-20090331 NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_assertion SIO_000772 12730697 NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_assertion evidence source_evidence_literature NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.
- NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_assertion description "[two mutations in the gene PCSK9 (encoding proprotein convertase subtilisin/kexin type 9) that cause autosomal dominant hypercholesterolemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199454.RAJvbL1Gb6g5iXR-3aXBuLTgGvWmj62M7knqYlRHIYONg130_provenance.