Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_assertion wasGeneratedBy ECO_0000218 NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_assertion wasDerivedFrom uniprot-2016 NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_assertion SIO_000772 19319977 NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_assertion evidence source_evidence_curated NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.
- NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_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." NP5743.RAEoaMGsW1BERFvW5QB3_LzLjY_d_C2ATcRW9nwx3J24k130_provenance.