Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_assertion description "[Mutations in CDKL5 and ARX are known causes of early-onset epilepsy and severe developmental delay in males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_assertion evidence source_evidence_literature NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_assertion SIO_000772 23583054 NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_assertion wasDerivedFrom befree-20140225 NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_assertion wasGeneratedBy ECO_0000203 NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP628396.RAF4Jrqo8YD_6O6zfLsw_n6qYMHCMyB-nr4KvvmuZ0JEw130_provenance.