Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_assertion description "[Thus, FXS can be considered a disorder of synaptic plasticity, and a developmental disorder in the purest sense: mutation of the FMR1 (fragile X mental retardation 1) gene results in abnormal synaptic development in response to experience.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_assertion evidence source_evidence_literature NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_assertion SIO_000772 21893938 NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_assertion wasDerivedFrom befree-2016 NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_assertion wasGeneratedBy ECO_0000203 NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.
- befree-2016 importedOn "2016-02-19" NP921571.RAZlKOf9knKOiDaeVM8WtjStnSdesWZR849xK6DyFqEak130_provenance.