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- NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_assertion type Assertion NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_head.
- NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_assertion description "[Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_provenance.
- NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_assertion evidence source_evidence_literature NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_provenance.
- NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_assertion SIO_000772 20298654 NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_provenance.
- NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_assertion wasDerivedFrom befree-20150227 NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_provenance.
- NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_assertion wasGeneratedBy ECO_0000203 NP836675.RAIK_o0LnNOKiEApjoQQ-0ruElFy8PqyIYl0asLs24prY130_provenance.