Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_assertion description "[A loss-of-function mutation in the FMR1 gene leads to subtle changes in neural development and subsequent mental impairment characteristic of FX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_assertion evidence source_evidence_literature NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_assertion SIO_000772 18225979 NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_assertion wasDerivedFrom befree-2016 NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_assertion wasGeneratedBy ECO_0000203 NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.
- befree-2016 importedOn "2016-02-19" NP652199.RAHLAbQVjRrYql_AIrG1Mf8Obwp41wAoRZYXO6kWkORPk130_provenance.