Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion> ?p ?o ?g. }
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- NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion type Assertion NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_head.
- NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion wasGeneratedBy ECO_0000203 NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_provenance.
- NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion wasDerivedFrom befree-2016 NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_provenance.
- NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion SIO_000772 11159940 NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_provenance.
- NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion evidence source_evidence_literature NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_provenance.
- NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_assertion description "[We have recently demonstrated that heterozygous mutations in the p63 gene are the major cause of EEC syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305680.RA-sDsaFreXZ1JhQrlyE-OpdmBJSUgcf1PTls40ZXuZSc130_provenance.