Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion description "[In this report, we describe a new murine model of the hereditary folate malabsorption syndrome that we developed through targeted disruption of the first 3 coding exons of the murine homolog of the PCFT gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion evidence source_evidence_literature NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion SIO_000772 21346251 NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion wasDerivedFrom befree-20150227 NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion wasGeneratedBy ECO_0000203 NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_provenance.