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- source_evidence_literature type ECO_0000212 NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_assertion description "[LAP2 mutations may represent a rare cause of DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_assertion evidence source_evidence_literature NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_assertion SIO_000772 16247757 NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_assertion wasDerivedFrom befree-20150227 NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_assertion wasGeneratedBy ECO_0000203 NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP469020.RAXtTPv5qwdrAYa5C0-JlKNQAdWsirDrkjV0wlnJy2lEE130_provenance.