Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion> ?p ?o ?g. }
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- NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion type Assertion NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_head.
- NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion description "[In this paper, we describe a boy with a 46,Y,der(X)t(X;Y)(p22.3;q11)mat karyotype and review the genotype-phenotype correlations in three male patients with the combination of apparent lack of clinical features of CDPX1 and a partial deletion of the critical region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_provenance.
- NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion evidence source_evidence_literature NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_provenance.
- NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion SIO_000772 7759082 NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_provenance.
- NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion wasDerivedFrom befree-20140225 NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_provenance.
- NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_assertion wasGeneratedBy ECO_0000203 NP517369.RAGFSZvU41kmFgA4W9iim2bv3sVY2nTmXRKYa00l-pwWo130_provenance.