Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion> ?p ?o ?g. }
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- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion type Assertion NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_head.
- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_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." NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_provenance.
- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion evidence source_evidence_literature NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_provenance.
- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion SIO_000772 11309367 NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_provenance.
- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion wasDerivedFrom befree-20140225 NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_provenance.
- NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_assertion wasGeneratedBy ECO_0000203 NP397026.RAVg3VqFyawXNsiGE_KqWs1NS5V7d10DTZCrAy08sFf9s130_provenance.