Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_assertion wasGeneratedBy ECO_0000218 NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_assertion wasDerivedFrom uniprot-2016 NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_assertion SIO_000772 21901787 NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_assertion evidence source_evidence_curated NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.
- NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_assertion description "[High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6768.RAEW2C8YD6fZV5QjUAch45l5XfTNLMG7bNml3F6P0uqBE130_provenance.