Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion wasGeneratedBy ECO_0000218 NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion wasDerivedFrom uniprot-20150221 NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion SIO_000772 19319977 NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion evidence source_evidence_curated NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.
- NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion description "[The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_provenance.