Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_assertion description "[Recent studies have implicated mutations in the ATP-binding cassette transporter A1, ABCA1, as a cause of Tangier disease (TD) and familial hypoalphalipoproteinemia (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_assertion evidence source_evidence_curated NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_assertion SIO_000772 14576201 NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_assertion wasDerivedFrom uniprot-20130724 NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_assertion wasGeneratedBy ECO_0000218 NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP19.RAPoYq1AP1xIR0of-SW0LnImjOpQl8HwPvb3bGs5iN4bM130_provenance.