Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion> ?p ?o ?g. }
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- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion type Assertion NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_head.
- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion wasGeneratedBy ECO_0000203 NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_provenance.
- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion wasDerivedFrom befree-20140225 NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_provenance.
- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion SIO_000772 22521702 NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_provenance.
- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_assertion evidence source_evidence_literature NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_provenance.
- NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_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." NP333290.RAq1zbaKHQfftCUrBK24tLwLbmR5Hu-x7ZawNJBhCtFxo130_provenance.