Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_assertion description "[Evaluation of genetic variation for E-selectin L554F polymorphisms revealed that the frequency of minor allele (F) and its heterozygous genotype (LF) is almost 4 times higher in the stroke patients than the controls (16.7 vs. 4.3 and 33.4 vs. 8.5, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_assertion evidence source_evidence_literature NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_assertion SIO_000772 19420919 NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_assertion wasDerivedFrom befree-2016 NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_assertion wasGeneratedBy ECO_0000203 NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.
- befree-2016 importedOn "2016-02-19" NP736999.RAjCPs7XHsonxl1evd8FRixgf_hX4DP3JDijdwGIdT1Gs130_provenance.