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- source_evidence_literature type ECO_0000212 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion description "[In one of the patients, the PRKAR1A gene responsible for Carney Complex and the KCNJ2 gene causal for Andersen syndrome are deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion evidence source_evidence_literature NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion SIO_000772 22166941 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion wasDerivedFrom befree-2016 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_assertion wasGeneratedBy ECO_0000203 NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP946386.RAB-KCVZ1nJzrF5KJmtv7S_-YHMTlzHmwvjX900gbFTxg130_provenance.