Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion> ?p ?o ?g. }
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- NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion type Assertion NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_head.
- NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion wasGeneratedBy ECO_0000203 NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_provenance.
- NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion wasDerivedFrom befree-20140225 NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_provenance.
- NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion SIO_000772 16429407 NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_provenance.
- NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion evidence source_evidence_literature NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_provenance.
- NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_assertion description "[The camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome is an autosomal recessive disorder caused by mutations in the PRG4 (Proteoglycan 4) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623281.RAih2Ze7rBS4TKverGXfh1aYSaNKKISvkF74En_QcmG7g130_provenance.