Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion> ?p ?o ?g. }
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- NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion type Assertion NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_head.
- NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion wasGeneratedBy ECO_0000203 NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_provenance.
- NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion wasDerivedFrom befree-20150227 NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_provenance.
- NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion SIO_000772 24127307 NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_provenance.
- NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion evidence source_evidence_literature NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_provenance.
- NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_assertion description "[One PHP-Ib patient showed a de novo microdeletion in STX16 and a loss of methylation of exon A/B on the maternal allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801779.RAHoyWdoIFr4EiAwIWHvMd5Up_WuUgEeQJ9nb_VpYYbdU130_provenance.