Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_assertion description "[GSTM1-null genotype or combination of the GSTM1-null and GSTT1-positive genotypes in females may be associated with increased risk of cataract development in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_assertion evidence source_evidence_literature NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_assertion SIO_000772 17514530 NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_assertion wasDerivedFrom lhgdn-20090331 NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_assertion wasGeneratedBy ECO_0000203 NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP135329.RAyw9S27kgtj0Al68CE7Evm10zyMf2xfNhmaI_xSfgbx0130_provenance.