Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion> ?p ?o ?g. }
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- NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_assertion type Assertion NP789.RA24Qj9WB8L1gEB9YQsJaw6vvw6WzcwPIYGvvpv7jM7yM130_head.
- 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.