Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion> ?p ?o ?g. }
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- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion type Assertion NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_head.
- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion wasGeneratedBy ECO_0000203 NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_provenance.
- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion wasDerivedFrom befree-20150227 NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_provenance.
- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion SIO_000772 22521702 NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_provenance.
- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_assertion evidence source_evidence_literature NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_provenance.
- NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_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." NP361896.RAcvL0RUvpzlEALBxWBj4L4_ekB-RRArwF0_ru348jnKk130_provenance.