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- source_evidence_literature type ECO_0000212 NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_assertion description "[Thus, the mislocalization of CLC-K2 was identified as the molecular pathogenesis of Bartter syndrome by mutant barttins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_assertion evidence source_evidence_literature NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_assertion SIO_000772 12761627 NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_assertion wasDerivedFrom befree-20140225 NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_assertion wasGeneratedBy ECO_0000203 NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859483.RAIpd5VD-WHpU16Bx7YDKxXOB9bKw8FfL6i2dHz1m2A0E130_provenance.