Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion> ?p ?o ?g. }
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- NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion type Assertion NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_head.
- NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion description "[Coffin-Siris Syndrome (CSS, MIM 135900) is a rare genetic disorder, and mutations in ARID1B were recently shown to cause CSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_provenance.
- NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion evidence source_evidence_literature NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_provenance.
- NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion SIO_000772 24569609 NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_provenance.
- NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion wasDerivedFrom befree-2016 NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_provenance.
- NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_assertion wasGeneratedBy ECO_0000203 NP1158125.RAM6TzKhL4c-426YqNN0M3smVvGF9Pl-EGNsmWDeAaWhs130_provenance.