Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- gad-20150221 importedOn "2015-02-21" NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_assertion wasGeneratedBy ECO_0000203 NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_assertion wasDerivedFrom gad-20150221 NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_assertion SIO_000772 19657220 NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_assertion evidence source_evidence_literature NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.
- NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_assertion description "[The percentage of N29I mutations in ACP patients was higher than that reported in other studies, while the percentage of N34S and AAT mutations in ACP and idiopathic CP patients was similar.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63490.RARYJU7_SsE_cQ67guNtvXet9huqS962LxvVdf_UdO940130_provenance.