Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion> ?p ?o ?g. }
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- NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion type Assertion NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_head.
- NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion description "[This finding makes the ARX dup24 mutation the most common mutation in nonsyndromic XLMR families linked to Xp22.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_provenance.
- NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion evidence source_evidence_literature NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_provenance.
- NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion SIO_000772 15850492 NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_provenance.
- NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion wasDerivedFrom befree-20140225 NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_provenance.
- NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_assertion wasGeneratedBy ECO_0000203 NP404734.RA5t4sdlWSOSxK2ybEwXzhpexBYT4r_18hD59FWo_D_Ug130_provenance.