Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_assertion evidence source_evidence_literature NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_assertion SIO_000772 22968132 NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_assertion wasDerivedFrom befree-20150227 NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_assertion wasGeneratedBy ECO_0000203 NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404333.RAwd34ngQfY2IIWQpar9Qt4svIdEzxatxELphuOnlXVk8130_provenance.