Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion> ?p ?o ?g. }
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- NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion type Assertion NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_head.
- NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion wasGeneratedBy ECO_0000203 NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_provenance.
- NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion wasDerivedFrom befree-20140225 NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_provenance.
- NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion SIO_000772 11886499 NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_provenance.
- NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion evidence source_evidence_literature NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_provenance.
- NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_assertion description "[Analysis of both phenotype and genotype data led to the following conclusions: (i) K6a or K16 mutations produce the pachyonychia congenita type 1 phenotype, whereas K17 (or K6b) mutations cause pachyonychia congenita type 2; (ii) the presence of pilosebaceous cysts following puberty is the best indicator of pachyonychia congenita type 2; (iii) prepubescent patients are more difficult to classify due to the lack of cysts; and (iv) natal teeth are indicative of pachyonychia congenita type 2, although their absence does not preclude the pachyonychia congenita type 2 phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311851.RAG8_1PQMsS_Z9YJPilUv0J6dkiC4sek_WekIdNT9fcVg130_provenance.