Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion> ?p ?o ?g. }
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- NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion type Assertion NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_head.
- NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion description "[Fragile X syndrome, the leading inherited cause of mental retardation and autism spectrum disorders worldwide, is caused by a tandem repeat expansion in the FMR1 (fragile X mental retardation 1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_provenance.
- NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion evidence source_evidence_literature NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_provenance.
- NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion SIO_000772 23719910 NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_provenance.
- NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion wasDerivedFrom befree-2016 NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_provenance.
- NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_assertion wasGeneratedBy ECO_0000203 NP1081765.RAbfV_JKTBkPY3itU2Xm6QWZ1vE4vT_sRGTLq2z8WwgOE130_provenance.