Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_assertion wasGeneratedBy ECO_0000203 NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_assertion wasDerivedFrom befree-20140225 NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_assertion SIO_000772 17276711 NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_assertion evidence source_evidence_literature NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_assertion description "[Rett syndrome (RS) is an X-linked dominant neurodevelopmental disorder caused by mutations in MECP2 (Xq28) and characterized by normal development until 6-12 months of age, followed by regression with loss of acquired skills, gradual onset of microcephaly, stereotypic hand movements and psychomotor delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP759830.RAy5rdEbNYSSXkagLo7jigqlljhHwv14yRIgC40qXJzAY130_provenance.