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- source_evidence_literature type ECO_0000212 NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_assertion description "[Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_assertion evidence source_evidence_literature NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_assertion SIO_000772 18229654 NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_assertion wasDerivedFrom befree-20150227 NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_assertion wasGeneratedBy ECO_0000203 NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277498.RAd3LLCp9IxM0alcyVicnc6P1GwJ6lgrggAhjcD2c7y4w130_provenance.