Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion> ?p ?o ?g. }
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- NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion type Assertion NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_head.
- NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion description "[Patients carrying the T(303)M mutation in the gene for matrilin-3 express a form of HOA that is radiologically indistinguishable from idiopathic HOA in individual patients but they have more severe thumb-base involvement, particularly in the STT joint.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_provenance.
- NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion evidence source_evidence_literature NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_provenance.
- NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion SIO_000772 16641049 NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_provenance.
- NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion wasDerivedFrom befree-20150227 NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_provenance.
- NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_assertion wasGeneratedBy ECO_0000203 NP546666.RAoFStoSn6xFE7hl1HzUMPXSQ-wLf_GqG2mmIwoEskSAE130_provenance.