Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_assertion description "[Allelic variations in the fms-like tyrosine kinase 1 and vascular endothelial growth factor C genes are associated with preeclampsia in both ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_assertion evidence source_evidence_literature NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_assertion SIO_000772 20223440 NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_assertion wasDerivedFrom gad-20150221 NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_assertion wasGeneratedBy ECO_0000203 NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.
- gad-20150221 importedOn "2015-02-21" NP167284.RAQ6W665i7QsDxXxVPK7UxUlZA_41ftScaXXLV2YMH-Do130_provenance.