Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_assertion wasGeneratedBy ECO_0000203 NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_assertion wasDerivedFrom befree-20150227 NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_assertion SIO_000772 15838369 NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_assertion evidence source_evidence_literature NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.
- NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_assertion description "[The risk for syncopes was associated with the (++) genotype of the ET-1 gene (P = 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364852.RAOrzpVZ-byPDcXxcGHLN8cnNo37nB4_eRlti8oX5l9Fc130_provenance.