Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion> ?p ?o ?g. }
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- NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion type Assertion NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_head.
- NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion description "[Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_provenance.
- NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion evidence source_evidence_literature NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_provenance.
- NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion SIO_000772 24095155 NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_provenance.
- NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion wasDerivedFrom befree-2016 NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_provenance.
- NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_assertion wasGeneratedBy ECO_0000203 NP1116265.RAX_qGqRxX7mX0fPuazMhWHzqgHqPLCRtRR0xtsEGgLvE130_provenance.