Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion type Assertion NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_head.
- NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion wasGeneratedBy ECO_0000218 NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_provenance.
- NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion wasDerivedFrom uniprot-20130724 NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_provenance.
- NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion SIO_000772 12730697 NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_provenance.
- NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion evidence source_evidence_curated NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_provenance.
- NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_assertion description "[Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4829.RAzEfvidq0goYUKK5PMmmqThBWeF-holoM2Rvd7R4JKgU130_provenance.