Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_assertion description "[Despite these figures, the screening of phaeochromocytomas and paragangliomas for mutations in the SDH genes to detect phaeochromocytoma-paraganglioma syndrome is rarely done because of time and financial constraints.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_assertion evidence source_evidence_literature NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_assertion SIO_000772 19576851 NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_assertion wasDerivedFrom befree-2016 NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_assertion wasGeneratedBy ECO_0000203 NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.
- befree-2016 importedOn "2016-02-19" NP749160.RAx2jQCBpN_T9m3WV0KnAA_Jrmy7UPwb-l17IBwOZAJEA130_provenance.