Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_assertion evidence source_evidence_literature NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_assertion SIO_000772 16211558 NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_assertion wasDerivedFrom gad-20150221 NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_assertion wasGeneratedBy ECO_0000203 NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.