Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_assertion description "[The haplotype analysis over the 45 Mb region, covering the linkage peak identified in Finnish MS families, revealed only modest association at IL7R (P = 0.04), recently implicated in MS, whereas most significant association was found with one haplotype covering the C7-FLJ40243 locus (P = 0.0001), 5.1 Mb centromeric of IL7R.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_assertion evidence source_evidence_literature NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_assertion SIO_000772 19221116 NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_assertion wasDerivedFrom befree-20140225 NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_assertion wasGeneratedBy ECO_0000203 NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.
- befree-20140225 importedOn "2014-02-25" NP263515.RAXVOv86_PRsEutr4XsLPS1FtROwS-HKVP7_NXFlfIzII130_provenance.