Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_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." NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_assertion evidence source_evidence_curated NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_assertion SIO_000772 9888420 NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_assertion wasDerivedFrom ctd_human-2016 NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_assertion wasGeneratedBy ECO_0000218 NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_provenance.