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- source_evidence_literature type ECO_0000212 NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_assertion description "[Methylmalonic aciduria (MMA) is an autosomal recessive inborn error of metabolism that results from functional defects in methylmalonyl CoA mutase (MCM), a nuclear-encoded, mitochondrial enzyme that uses the vitamin B12 derivative, adenosylcobalamin (AdoCbl) as a cofactor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_assertion evidence source_evidence_literature NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_assertion SIO_000772 9554742 NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_assertion wasDerivedFrom befree-20140225 NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_assertion wasGeneratedBy ECO_0000203 NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610963.RAiRG9B5aYg_il4pTN1FxdOjsEy0Zf7WC0T6kIqkKhAzs130_provenance.