Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_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 disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_assertion evidence source_evidence_literature NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_assertion SIO_000772 20398908 NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_assertion wasDerivedFrom gad-20130706 NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_assertion wasGeneratedBy ECO_0000203 NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86859.RAOG85CzZdXCQgP1bn67Zo3RnrcKQCXxXvSI0eQBMpC2c130_provenance.