Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_assertion description "[MTHFR gene mutation was evaluated in patients with severe pregnancy complications in northern Finland/mutation was homozygous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_assertion evidence source_evidence_literature NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_assertion SIO_000772 16514238 NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_assertion wasDerivedFrom lhgdn-20090331 NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_assertion wasGeneratedBy ECO_0000203 NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215892.RAFYN-UTftwJs1UXvKZgsZa6N2ILP6UVjK64yJ636gLLQ130_provenance.