Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_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." NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_assertion evidence source_evidence_curated NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_assertion SIO_000772 16030523 NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_assertion wasDerivedFrom ctd_human-20130708 NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_assertion wasGeneratedBy ECO_0000218 NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP21807.RAre_uU5vhakY0nCiMuPGwH4fZlN6CTeFRSkEoto8Gbv0130_provenance.