Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_assertion wasGeneratedBy ECO_0000203 NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_assertion wasDerivedFrom befree-20150227 NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_assertion SIO_000772 22998673 NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_assertion evidence source_evidence_literature NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.
- NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_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." NP719356.RAdGQHNxNRxrN5BF1hAH8ndLZKfv0nKzTDGN2dZeX1Ni4130_provenance.