Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_assertion wasGeneratedBy ECO_0000203 NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_assertion wasDerivedFrom befree-20150227 NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_assertion SIO_000772 10818218 NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_assertion evidence source_evidence_literature NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.
- NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_assertion description "[The aim of this population screening study was to determine if Fra-X or FRAXE mutations are the cause of a number of cases of mental retardation in a sample of Mexican children with mental retardation of unknown cause (MRUC) and to stress the importance of performing molecular analysis of the FMR-1 gene in all patients with MRUC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409171.RAxHc6LaeytlNjdTgnbwj8FOaD3_vBCJ1Zo1I8Mb3PypM130_provenance.