Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion> ?p ?o ?g. }
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- NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion type Assertion NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_head.
- NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion description "[Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare heritable disorder of connective tissue characterized by congenital malformations of the great toes and recurrent episodes of painful soft tissue swelling that lead to heterotopic ossifications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_provenance.
- NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion evidence source_evidence_literature NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_provenance.
- NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion SIO_000772 19300893 NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_provenance.
- NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion wasDerivedFrom befree-20140225 NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_provenance.
- NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_assertion wasGeneratedBy ECO_0000203 NP861462.RAfsL2xRReNPaBYa169TqCNRr8gslA2P5prodtP3pmN1I130_provenance.