Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_assertion description "[Fragile X syndrome, the leading inherited cause of mental retardation and autism spectrum disorders worldwide, is caused by a tandem repeat expansion in the FMR1 (fragile X mental retardation 1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_assertion evidence source_evidence_literature NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_assertion SIO_000772 23719910 NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_assertion wasDerivedFrom befree-20140225 NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_assertion wasGeneratedBy ECO_0000203 NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624699.RAFOO70SOnveFptxGQLajo3HkZhX08DAilQSevSzSiNzE130_provenance.