Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion> ?p ?o ?g. }
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- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion type Assertion NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_head.
- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion description "[These findings, with the compelling genetic evidence suggesting the presence in Xq28 of additional genes besides RabGDI1 and FMR2 involved in non-specific X-linked mental retardation (MRX), prompted us to investigate MECP2 in MRX families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_provenance.
- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion evidence source_evidence_literature NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_provenance.
- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion SIO_000772 11309367 NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_provenance.
- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion wasDerivedFrom befree-20150227 NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_provenance.
- NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_assertion wasGeneratedBy ECO_0000203 NP412877.RAMZw1b2icOST2P7kwFzFFlNXXVmZnChAgeQqwFM3V6R8130_provenance.