Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_assertion description "[Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked neurodevelopmental disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_assertion evidence source_evidence_literature NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_assertion SIO_000772 17486179 NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_assertion wasDerivedFrom befree-2016 NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_assertion wasGeneratedBy ECO_0000203 NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP608745.RANWwjjBRuBvuFt4k5hu-S46BuhTUL3ZlLmEJd8wJ0V_Y130_provenance.