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- source_evidence_literature type ECO_0000212 NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_assertion description "[The frequency of PRSS1 mutation was present in 21.4% of ICP patients, which was significantly higher (p < 0.05) than in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_assertion evidence source_evidence_literature NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_assertion SIO_000772 20676769 NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_assertion wasDerivedFrom befree-2016 NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_assertion wasGeneratedBy ECO_0000203 NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.
- befree-2016 importedOn "2016-02-19" NP829981.RAWCH8G3KBriySOxlq9tNo8oxVR45d0e9nRxkanlJSnvE130_provenance.