Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion> ?p ?o ?g. }
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- NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion type Assertion NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_head.
- NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion wasGeneratedBy ECO_0000218 NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_provenance.
- NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion wasDerivedFrom uniprot-20130724 NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_provenance.
- NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion SIO_000772 9767294 NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_provenance.
- NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion evidence source_evidence_curated NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_provenance.
- NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_assertion description "[Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3612.RAIhOyyww6FT0GyAilGQJB9GLFrpTQSWoYpRqV69d4Iy0130_provenance.