Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion> ?p ?o ?g. }
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- NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_assertion type Assertion NP28281.RAcfcwIUQxLvTQE2JkEliuxLhfe-NkYe3_WxTDeeaNxNg130_head.
- 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.