Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_assertion description "[We review cases with cytogenetic anomalies involving 8p23.1, discuss a potential relationship between 8p23.1 deletions and CdLS and suggest a novel candidate gene for CdLS-Tankyrase 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_assertion evidence source_evidence_literature NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_assertion SIO_000772 18470924 NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_assertion wasDerivedFrom befree-2016 NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_assertion wasGeneratedBy ECO_0000203 NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.
- befree-2016 importedOn "2016-02-19" NP670301.RAGLJIyFy_UI_BmRWFIlIsZ_VK37BFUeWOzl-as9h0Cq0130_provenance.