Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_assertion description "[Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_assertion evidence source_evidence_literature NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_assertion SIO_000772 23043934 NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_assertion wasDerivedFrom befree-20140225 NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_assertion wasGeneratedBy ECO_0000203 NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP634543.RAhoHbDJKqnKJLOvnkg5mtB4gkulp6Vc5OP3kPWy5G8sA130_provenance.