Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_assertion description "[PCDH19 is expressed in developing brains of human and mouse and is the first member of the cadherin superfamily to be directly implicated in epilepsy or mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_assertion evidence source_evidence_literature NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_assertion SIO_000772 18469813 NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_assertion wasDerivedFrom befree-2016 NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_assertion wasGeneratedBy ECO_0000203 NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.
- befree-2016 importedOn "2016-02-19" NP670251.RAxzoaM65KiYvqvCntV_kYJxb-x6Lv7rx4uG-f5FXFkRk130_provenance.