Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion> ?p ?o ?g. }
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- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion type Assertion NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_head.
- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_provenance.
- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion evidence source_evidence_literature NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_provenance.
- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion SIO_000772 10644430 NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_provenance.
- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion wasDerivedFrom befree-2016 NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_provenance.
- NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_assertion wasGeneratedBy ECO_0000203 NP273065.RAH_BUTH1hkrM3iI-6nogLMNg-vdxGiNMHBCMDSx7IJ20130_provenance.