Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_assertion description "[Re-assigned diagnosis of D4ST1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) after initial diagnosis of Marden-Walker syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_assertion evidence source_evidence_literature NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_assertion SIO_000772 22987394 NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_assertion wasDerivedFrom befree-20150227 NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_assertion wasGeneratedBy ECO_0000203 NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964096.RAmhzQ1sPMDNI6845Ovj-cARXjdlCU-qxSc-ywCjXcUAU130_provenance.