Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion description "[Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion evidence source_evidence_literature NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion SIO_000772 16647848 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion wasDerivedFrom befree-2016 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_assertion wasGeneratedBy ECO_0000203 NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.
- befree-2016 importedOn "2016-02-19" NP547445.RAozVu1gHdULzxx95tN2w-pFm41eKOfy-v0SopfD4ZNxs130_provenance.