Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_assertion> ?p ?o ?g. }
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- NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_assertion type Assertion NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_head.
- NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_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." NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_provenance.
- NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_assertion evidence source_evidence_literature NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_provenance.
- NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_assertion SIO_000772 12525535 NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_provenance.
- NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_assertion wasDerivedFrom befree-20150227 NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_provenance.
- NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_assertion wasGeneratedBy ECO_0000203 NP320132.RAPXVxZjRUBZzZVqaVeu7uhoalTejGgI2OAOPTPEHa7io130_provenance.