Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_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." NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_assertion evidence source_evidence_literature NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_assertion SIO_000772 17514530 NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_assertion wasDerivedFrom lhgdn-20090331 NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_assertion wasGeneratedBy ECO_0000203 NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP225422.RAC2WgRo3SX1mWunwvfqBTfkmLHCQ07oGznSymdKqT0cg130_provenance.