Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric diso]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_assertion evidence source_evidence_literature NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_assertion SIO_000772 20398908 NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_assertion wasDerivedFrom gad-20150221 NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_assertion wasGeneratedBy ECO_0000203 NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP172971.RAEMD-SLSW_gT-kTFyINmsLAg7lXCkJLeaXiA3KfZGN8U130_provenance.