Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion> ?p ?o ?g. }
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- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion type Assertion NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_head.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion evidence source_evidence_literature NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion SIO_000772 16000300 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion wasDerivedFrom befree-20140225 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion wasGeneratedBy ECO_0000203 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.