Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion> ?p ?o ?g. }
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- NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion type Assertion NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_head.
- NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion description "[About 30% of the mutations causing nonsyndromic X-linked mental retardation (MRX) are thought to be located in Xp11 and in the pericentromeric region, with a particular clustering of gene defects in a 7.4 Mb interval flanked by the genes ELK1 and ALAS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_provenance.
- NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion evidence source_evidence_literature NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_provenance.
- NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion SIO_000772 16969374 NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_provenance.
- NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion wasDerivedFrom befree-2016 NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_provenance.
- NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_assertion wasGeneratedBy ECO_0000203 NP569094.RAeRtj1ANKVReP_SIKcjFtFt3fi87KeobGzOT6VSCGqas130_provenance.