Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_assertion description "[The genotyping results of the 18 heterozygous subjects and 12 wild-type subjects were validated by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_assertion evidence source_evidence_literature NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_assertion SIO_000772 15684873 NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_assertion wasDerivedFrom gad-20150221 NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_assertion wasGeneratedBy ECO_0000203 NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90363.RAYhqlm-DGpnXbw_YhDMWTI0RII2sF1BeIdQ_P1OPh8fg130_provenance.