Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_assertion description "[MECP2 mutations cause the X-linked neurodevelopmental disorder Rett Syndrome (RTT) by consistently altering the protein encoded by the MECP2e1 alternative transcript.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_assertion evidence source_evidence_literature NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_assertion SIO_000772 25644311 NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_assertion wasDerivedFrom befree-2016 NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_assertion wasGeneratedBy ECO_0000203 NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260357.RAt9NxHJM-_FEM55ovNQ-HNkTOxYYDwRTyD3-dMOygpfs130_provenance.