Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion> ?p ?o ?g. }
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- NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion type Assertion NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_head.
- NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion description "[Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_provenance.
- NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion evidence source_evidence_literature NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_provenance.
- NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion SIO_000772 15805154 NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_provenance.
- NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion wasDerivedFrom befree-20150227 NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_provenance.
- NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_assertion wasGeneratedBy ECO_0000203 NP300016.RAmwa3Ipy1J92uRoytke7uzB8wLGSMY7kyhvfQ0RHVGgc130_provenance.