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- NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_assertion type Assertion NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_head.
- NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_assertion description "[20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_provenance.
- NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_assertion evidence source_evidence_literature NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_provenance.
- NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_assertion SIO_000772 23262345 NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_provenance.
- NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_assertion wasDerivedFrom befree-2016 NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_provenance.
- NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_assertion wasGeneratedBy ECO_0000203 NP1038145.RAv8XsuYtdixeOtFNMKRNS7nd7KqljfcBHZBGSFV2_Dpg130_provenance.