Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_assertion description "[Over the last several years, intragenic or genomic alterations of the CDKL5 and FOXG1 genes have been associated with severe cognitive impairment, early onset epilepsy and, often, dyskinetic movement disorders, which have variably been defined as Rett variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_assertion evidence source_evidence_literature NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_assertion SIO_000772 22998673 NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_assertion wasDerivedFrom befree-2016 NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_assertion wasGeneratedBy ECO_0000203 NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1014883.RAjliEl7suJJJkOl4XabnUzPFA7lKR25XdKuy4MV6mtyY130_provenance.