Matches in Nanopublications for { ?s ?p "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP642943.RAlDXsgLMqx6qLJo6vNw3bNVsygi1gSxHyCaCwmpILyWw130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642943.RAlDXsgLMqx6qLJo6vNw3bNVsygi1gSxHyCaCwmpILyWw130_provenance.
- NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_provenance.
- NP846801.RAcrnEAV-WnLX6Is697Ih5xC715FJfwbzcancQqF8pI3c130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846801.RAcrnEAV-WnLX6Is697Ih5xC715FJfwbzcancQqF8pI3c130_provenance.
- NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- NP483633.RAwLlTXxFd-I5RwgFKyANNNDIq6coofR-GytJujnJKrCo130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483633.RAwLlTXxFd-I5RwgFKyANNNDIq6coofR-GytJujnJKrCo130_provenance.
- NP884449.RATzj9-mPyf4VuuP-IpWRKvOQ3D2P7qsH-8VEG0R6wZoA130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884449.RATzj9-mPyf4VuuP-IpWRKvOQ3D2P7qsH-8VEG0R6wZoA130_provenance.
- NP192344.RA-9INDP3fQ9uUWM83rSA45bQk7_6QMNnCBArnMubhiNI130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192344.RA-9INDP3fQ9uUWM83rSA45bQk7_6QMNnCBArnMubhiNI130_provenance.
- NP865352.RA-m189RvDw3vV1EDnGXTJAXMIRRr5TGDBBHL1M1RGJqA130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865352.RA-m189RvDw3vV1EDnGXTJAXMIRRr5TGDBBHL1M1RGJqA130_provenance.