Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion> ?p ?o ?g. }
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- NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion type Assertion NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_head.
- NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion description "[In the last year or so, mutations were discovered in differentiation specific keratins K6a and K16 causing pachyonychia congenita type 1 and K17 mutations occur in pachyonychia congenita type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_provenance.
- NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion evidence source_evidence_literature NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_provenance.
- NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion SIO_000772 9028791 NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_provenance.
- NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion wasDerivedFrom befree-20140225 NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_provenance.
- NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_assertion wasGeneratedBy ECO_0000203 NP456196.RAj0ehGLDzWpIJP8WwDMpOg9IZxZ_1QWtQtKgJR-CWSRY130_provenance.