Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_assertion wasGeneratedBy ECO_0000203 NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_assertion wasDerivedFrom gad-20150221 NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_assertion SIO_000772 11904677 NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_assertion evidence source_evidence_literature NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.
- NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_assertion description "[A majority of the north Indian KIR gene profiles have not been seen in Caucasian and Asian populations. Most striking is a higher frequency of the B group of KIR haplotypes, resulting in equal frequencies for A and B group haplotypes in north Indians. All]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70089.RAv3xfs_skenP1L7yz0MkbJSi8Na1lH-QruXcnJHyT1ZU130_provenance.