Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_assertion description "[Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_assertion evidence source_evidence_literature NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_assertion SIO_000772 25105228 NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_assertion wasDerivedFrom befree-2016 NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_assertion wasGeneratedBy ECO_0000203 NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1208831.RAvFvbgoRFrRN0GiOrAa79FUm3uKRGS7kEuSmycGLnVKg130_provenance.