Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_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." NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_assertion evidence source_evidence_literature NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_assertion SIO_000772 16372906 NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_assertion wasDerivedFrom befree-20150227 NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_assertion wasGeneratedBy ECO_0000203 NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP574879.RAKLoFCpCIIKPeNpNgdwRsCFWNcy5Qr8waneU9cqnxr-Q130_provenance.