Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion description "[Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion evidence source_evidence_curated NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion SIO_000772 9888420 NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion wasDerivedFrom ctd_human-20130708 NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion wasGeneratedBy ECO_0000218 NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_provenance.