Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_assertion description "[We investigated 29 single nucleotide polymorphisms (SNPs) within the P2RX7 gene and adjacent genes in a sample of 1000 German Caucasian patients suffering from recurrent major depressive disorder (MDD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_assertion evidence source_evidence_literature NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_assertion SIO_000772 16822851 NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_assertion wasDerivedFrom befree-20140225 NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_assertion wasGeneratedBy ECO_0000203 NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP652887.RANtFyoWBpZT561iGzovaXgFpKGcWtkneUcs10TkjjDEg130_provenance.