Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion> ?p ?o ?g. }
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- NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion type Assertion NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_head.
- NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion description "[The Fragile X-Related 1 gene (FXR1) is a paralog of the Fragile X Mental Retardation 1 gene (FMR1), whose absence causes the Fragile X syndrome, the most common form of inherited intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_provenance.
- NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion evidence source_evidence_literature NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_provenance.
- NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion SIO_000772 23555284 NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_provenance.
- NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion wasDerivedFrom befree-2016 NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_provenance.
- NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_assertion wasGeneratedBy ECO_0000203 NP1066299.RATHHcTVG6elxJ9Vcl4Nq0GRC41INAX7wJcchzWzg8okg130_provenance.