Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_assertion description "[These findings indicate that MHS-related RYR1 mutations may present later in life with prominent axial weakness but not always typical histopathological features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_assertion evidence source_evidence_literature NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_assertion SIO_000772 23329375 NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_assertion wasDerivedFrom befree-20140225 NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_assertion wasGeneratedBy ECO_0000203 NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP629145.RAzgSq_eRt32vZdsjhwep04HqTe6PqzbhgZOApEliClg4130_provenance.