Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_assertion> ?p ?o ?g. }
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- NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_assertion type Assertion NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_head.
- NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_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." NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_provenance.
- NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_assertion evidence source_evidence_literature NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_provenance.
- NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_assertion SIO_000772 16969374 NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_provenance.
- NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_assertion wasDerivedFrom befree-20150227 NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_provenance.
- NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_assertion wasGeneratedBy ECO_0000203 NP970817.RAy9DvKoVMdL1tC4yuvt5tN2ioZFA-DVl9Zg2QCKzNbgg130_provenance.