Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_assertion> ?p ?o ?g. }
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- NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_assertion type Assertion NP38065.RA4mfCgsMJQg7Z3O08Csa1JKbxXzdNNDbsX7LkdUoKyXw130_head.
- 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.