Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_assertion description "[Genetic variation within ACVR1 is associated with AMH levels and follicle number in PCOS women, suggesting that ALK2 signalling contributes to the disturbed folliculogenesis in PCOS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_assertion evidence source_evidence_literature NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_assertion SIO_000772 18854405 NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_assertion wasDerivedFrom gad-20130706 NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_assertion wasGeneratedBy ECO_0000203 NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP78525.RAvlQH_SiJDbiNHtGFjcwan9KOIlolcBrWHoVGAj3sMQM130_provenance.