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- source_evidence_literature type ECO_0000212 NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- befree-2016 importedOn "2016-02-19" NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_assertion wasGeneratedBy ECO_0000203 NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_assertion wasDerivedFrom befree-2016 NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_assertion SIO_000772 18989701 NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_assertion evidence source_evidence_literature NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.
- NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702064.RAASSRpqRblS-TeoxV5KODJVkEh8tbVL02td-mbUZwA48130_provenance.