Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_assertion description "[Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2 gene (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_assertion evidence source_evidence_literature NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_assertion SIO_000772 21940684 NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_assertion wasDerivedFrom befree-2016 NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_assertion wasGeneratedBy ECO_0000203 NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.
- befree-2016 importedOn "2016-02-19" NP925788.RASWHYVeJHQlLXQr8yREgPEGAV0Y7Z0_YbwV1LmUMumoE130_provenance.