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- source_evidence_literature type ECO_0000212 NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_assertion evidence source_evidence_literature NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_assertion SIO_000772 19369868 NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_assertion wasDerivedFrom befree-20150227 NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_assertion wasGeneratedBy ECO_0000203 NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP828681.RAtw1NIwJGrxZnGcjasRBVa6JFElSBiuW-_6l-yNE4MJU130_provenance.