Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_assertion description "[(The MTHFR 677 T allele frequency was not different in DS cases and case mothers, compared to the respective control groups).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_assertion evidence source_evidence_literature NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_assertion SIO_000772 12923861 NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_assertion wasDerivedFrom befree-20140225 NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_assertion wasGeneratedBy ECO_0000203 NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP270059.RAV3_iffm0EnTS8EoPNpc2SDCOSHpQh43bStgfURsBuwQ130_provenance.