Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_assertion description "[The frequency of minor allele (R) and heterozygous (RS) genotype of E-selectin S128R polymorphism was significantly higher in the stroke patients than in the controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_assertion evidence source_evidence_literature NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_assertion SIO_000772 19420919 NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_assertion wasDerivedFrom gad-20130706 NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_assertion wasGeneratedBy ECO_0000203 NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP81786.RAho20UMHyMZN1viv0WAq2uFGwTfnFOLy611mibz6NcmI130_provenance.