Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_assertion description "[An insertion/deletion polymorphism in the angiotensin converting enzyme gene is associated with both brain substance P contents and affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_assertion evidence source_evidence_literature NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_assertion SIO_000772 8931914 NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_assertion wasDerivedFrom gad-20130706 NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_assertion wasGeneratedBy ECO_0000203 NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49637.RAKdhA9hB-rnArbaYAMP5shrw9XAm1fBGM1C-Y9XxrLFE130_provenance.