Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_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." NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_assertion evidence source_evidence_literature NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_assertion SIO_000772 18225979 NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_assertion wasDerivedFrom befree-20150227 NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_assertion wasGeneratedBy ECO_0000203 NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409080.RACp5djzGMqC-eOzG3sc28BrX6CkAFR_wJDZFjePiqBgY130_provenance.