Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_assertion description "[A cohort of 1002 heterozygous FH patients was genotyped for polymorphisms in the genes encoding for ATP-binding cassette transporter A1, apolipoprotein (apo) AIV, apoCIII, apoE, cholesteryl transfer ester protein, hepatic lipase, lipoprotein lipase, and two paraoxonases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_assertion evidence source_evidence_curated NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_assertion SIO_000772 16030523 NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_assertion wasDerivedFrom ctd_human-20150221 NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_assertion wasGeneratedBy ECO_0000218 NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP7169.RAmatSYlvbazu9FWL3wGiyC7v0K-FIuLrmGTNcpN93fi8130_provenance.