Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_assertion description "[RET deletion was exclusive to seven cases, and RIT2 deletions were overrepresented common variant CNVs in the schizophrenia cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_assertion evidence source_evidence_literature NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_assertion SIO_000772 20489179 NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_assertion wasDerivedFrom gad-20150221 NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_assertion wasGeneratedBy ECO_0000203 NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP127332.RAQoiAygmBt4QfdFot1YDp89PTtK8HNfLAYvhQ-25tRXE130_provenance.