Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_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." NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_assertion evidence source_evidence_literature NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_assertion SIO_000772 18225979 NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_assertion wasDerivedFrom befree-20140225 NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_assertion wasGeneratedBy ECO_0000203 NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP824655.RA4Z6pYa1GPC5w5Bl2xOtXWjma7cfF1C0etj3eNafTXTA130_provenance.