Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_assertion type Assertion NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_head.
- NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_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." NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_provenance.
- NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_assertion evidence source_evidence_literature NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_provenance.
- NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_assertion SIO_000772 16211558 NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_provenance.
- NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_assertion wasDerivedFrom lhgdn-20090331 NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_provenance.
- NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_assertion wasGeneratedBy ECO_0000203 NP197923.RA_qbZkHs4SKGOYSIUuNHmtnYw7A-KGn-HAYrhvsCdZVs130_provenance.