Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion> ?p ?o ?g. }
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- NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion type Assertion NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_head.
- NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion description "[Loss-of-function mutations in the FLG (filaggrin) gene cause the semidominant keratinizing disorder ichthyosis vulgaris and convey major genetic risk for atopic dermatitis (eczema), eczema-associated asthma and other allergic phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_provenance.
- NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion evidence source_evidence_curated NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_provenance.
- NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion SIO_000772 19349982 NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_provenance.
- NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion wasDerivedFrom ctd_human-20130708 NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_provenance.
- NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_assertion wasGeneratedBy ECO_0000218 NP15921.RAAuTFhNzpJMExX3Bc-TJMinSAgrYmAe0mvdW6n227raM130_provenance.