Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion type Assertion NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_head.
- NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion description "[The gene encoding fatty acid CoA ligase 4 (FACL4) is mutated in families with non-specific X linked mental retardation (MRX) and is responsible for cognitive impairment in the contiguous gene syndrome ATS-MR (Alport syndrome and mental retardation), mapped to Xq22.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_provenance.
- NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion evidence source_evidence_literature NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_provenance.
- NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion SIO_000772 12525535 NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_provenance.
- NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion wasDerivedFrom befree-20140225 NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_provenance.
- NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_assertion wasGeneratedBy ECO_0000203 NP691991.RA2hhSL3FLfyhuzrKrPRzrjzu-6bIrbEO9ICAfVC2rgJU130_provenance.