Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_assertion description "[Mutations of the protocadherin19 gene (PCDH19) cause a female-related epilepsy of variable severity, with or without mental retardation and autistic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_assertion evidence source_evidence_literature NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_assertion SIO_000772 22946748 NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_assertion wasDerivedFrom befree-20140225 NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_assertion wasGeneratedBy ECO_0000203 NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP777906.RA_POjEXTId79KkkHJLw_yKGxrAewa-PhdzwNtYAcOAfY130_provenance.