Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion> ?p ?o ?g. }
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- NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion type Assertion NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_head.
- NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion description "[Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_provenance.
- NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion evidence source_evidence_literature NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_provenance.
- NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion SIO_000772 23830518 NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_provenance.
- NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion wasDerivedFrom befree-2016 NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_provenance.
- NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_assertion wasGeneratedBy ECO_0000203 NP1091759.RAbRdRxKjFXcbb0ghec9vfVzREiLEBp3yDRPpTMuAs_Eg130_provenance.