Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_assertion description "[Recently, suggestive association has been reported between a single nucleotide polymorphism (SNP; rs1801131, also known as A1298C) in the methyltetrahydrofolate reductase (MTHFR) gene and AO of HD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_assertion evidence source_evidence_literature NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_assertion SIO_000772 16372906 NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_assertion wasDerivedFrom befree-2016 NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_assertion wasGeneratedBy ECO_0000203 NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP528139.RAfrHf6Xt4UJDKBo5_WdzDtHC6rhsTYTC0yOx-hgd5kOQ130_provenance.