Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_assertion description "[The insertion-deletion polymorphism in intron 1 of the gamma 2 actin gene is unlikely to play any significant role in obstetric cholestasis or preeclampsia in patients from eastern Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_assertion evidence source_evidence_literature NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_assertion SIO_000772 17934296 NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_assertion wasDerivedFrom lhgdn-20090331 NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_assertion wasGeneratedBy ECO_0000203 NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP194982.RA4pG6MUPfPorAV1xOX2r_mLw-TV6YS6_mtNKyT2HxNak130_provenance.