Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion type Assertion NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_head.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_provenance.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion evidence source_evidence_literature NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_provenance.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion SIO_000772 19206178 NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_provenance.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion wasDerivedFrom befree-20140225 NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_provenance.
- NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_assertion wasGeneratedBy ECO_0000203 NP683792.RAJkJZL2YlFTjGf39JCT634JJoPybn_6iMwBqevEiSj10130_provenance.