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- source_evidence_literature type ECO_0000212 NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_assertion description "[We found a trend toward an increased risk of migraine in subjects carrying a homozygous mutant genotype for MTHFR C677T and MTHFR A1298C polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_assertion evidence source_evidence_literature NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_assertion SIO_000772 16686913 NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_assertion wasDerivedFrom befree-2016 NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_assertion wasGeneratedBy ECO_0000203 NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.
- befree-2016 importedOn "2016-02-19" NP549066.RAahRc_QpLB3wDtGvVSPnV9olevHXH9gQKyLQNGQkh-8I130_provenance.