Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion> ?p ?o ?g. }
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- NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion type Assertion NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_head.
- 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.
- NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion evidence source_evidence_literature NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_provenance.
- NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion SIO_000772 17719747 NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_provenance.
- NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion wasDerivedFrom befree-20140225 NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_provenance.
- NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_assertion wasGeneratedBy ECO_0000203 NP612097.RATxB3U3Jd4ee5cqg5p55oqtj-sK3AsbKIv6QEKMAr9os130_provenance.