Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_assertion description "[Methylenetetrahydrofolate reductase polymorphisms C677T and risk of autism in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_assertion evidence source_evidence_literature NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_assertion SIO_000772 22775456 NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_assertion wasDerivedFrom befree-20150227 NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_assertion wasGeneratedBy ECO_0000203 NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP574419.RAPij069EhYyW0RQqoQ991lUmzzwVrL6GDJ2BfVJ-hXpU130_provenance.