Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_assertion description "[Recent studies suggest an association between the EPHX1 codon 113 polymorphism or homozygous null GSTM1 allele and the risk of carcinogenesis, emphysema, phenytoin-associated oral clefting, and the risk of spontaneous abortion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_assertion evidence source_evidence_literature NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_assertion SIO_000772 11471167 NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_assertion wasDerivedFrom befree-20140225 NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_assertion wasGeneratedBy ECO_0000203 NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP565832.RADZu0bhlLEIBm3KFWUevkNA9yAGgbG4IKhiypTrbXHFE130_provenance.