Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_assertion description "[Patients with the CDKL5 mutation have an early onset, epileptic encephalopathy in infancy that evolves into myoclonic seizures in childhood with a unique EEG pattern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_assertion evidence source_evidence_literature NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_assertion SIO_000772 16326141 NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_assertion wasDerivedFrom befree-20150227 NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_assertion wasGeneratedBy ECO_0000203 NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719286.RASo_kpQrHh-EEc9BP3JhP82sMO1-HPZIiPem32DaHtWU130_provenance.