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- source_evidence_literature type ECO_0000212 NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_assertion description "[Mutations in PRKAG2 have been described in patients with familial WPW syndrome and hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_assertion evidence source_evidence_literature NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_assertion SIO_000772 18812404 NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_assertion wasDerivedFrom befree-20150227 NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_assertion wasGeneratedBy ECO_0000203 NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP905608.RAFstjPU9etjh_DiJ9B3PeUgypqoOqc47YVjIT6f6lEqw130_provenance.