Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_assertion description "[analysis of MCAD deficiency (homozygous at c.985A > G (K329E)) complicated by acute liver failure in pregnancy [case report]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_assertion evidence source_evidence_literature NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_assertion SIO_000772 17186412 NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_assertion wasDerivedFrom lhgdn-20090331 NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_assertion wasGeneratedBy ECO_0000203 NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP149665.RAyLc8bfB9B37dC8raPdhWolPDRWDXT9HF9_3K0I8ogMQ130_provenance.