Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion> ?p ?o ?g. }
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- NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_assertion type Assertion NP964124.RA_mgFJ_5BVibGxD8ihV1aLLvQihb23UDmX9P1aT0dXHc130_head.
- 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.