Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_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." NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_assertion evidence source_evidence_literature NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_assertion SIO_000772 19420919 NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_assertion wasDerivedFrom befree-20140225 NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_assertion wasGeneratedBy ECO_0000203 NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP588113.RArNWrTdPAyBZ3oxplGK5DHW7kODATV5Lg6teoVbUdIa8130_provenance.