Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_assertion description "[A high-density genotyping array (50K IBC Chip) containing single-nucleotide polymorphisms (SNPs) from E-selectin candidate genes selected on known biology of E-selectin metabolism, mouse genetic studies, and human genetic association studies, was used for genotyping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_assertion evidence source_evidence_literature NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_assertion SIO_000772 23300549 NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_assertion wasDerivedFrom befree-20140225 NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_assertion wasGeneratedBy ECO_0000203 NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP636327.RA98E9NuH2loFhvnnRplzUGWKSOcu4wOITT0_jNOBalqE130_provenance.