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- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_assertion type Assertion NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_head.
- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_assertion wasGeneratedBy ECO_0000203 NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_provenance.
- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_assertion wasDerivedFrom befree-2016 NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_provenance.
- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_assertion SIO_000772 22521702 NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_provenance.
- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_assertion evidence source_evidence_literature NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_provenance.
- NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_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." NP976381.RADwixbAuqUMypRr8qUbaGm2touXf7j2L536MHerOKJb0130_provenance.