Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion> ?p ?o ?g. }
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- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion type Assertion NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_head.
- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion wasGeneratedBy ECO_0000203 NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_provenance.
- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion wasDerivedFrom befree-2016 NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_provenance.
- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion SIO_000772 22521702 NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_provenance.
- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion evidence source_evidence_literature NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_provenance.
- NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_assertion description "[Hereditary dentine disorders dentinogenesis imperfecta type II/III and dentine dysplasia are currently proposed to be one disease with distinct clinical manifestations reflecting various mutations in the same DSPP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976382.RA6AoSBq--AyN7MODO3qCGs_rVgimZcWV_OlZ253fwKtg130_provenance.