Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_assertion description "[A single nucleotide polymorphism variant within the general transcription factor IIH, polypeptide 4 gene, GTF2H4, on chromosome 6p21.33 was significantly associated with MS (odds ratio = 0.7, P = 3.5 x 10(-5)) after accounting for multiple testing and was not due to linkage disequilibrium with HLA-DRB1*1501.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_assertion evidence source_evidence_literature NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_assertion SIO_000772 20522537 NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_assertion wasDerivedFrom gad-20130706 NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_assertion wasGeneratedBy ECO_0000203 NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86893.RAelMfshmTY1rHLFZb_dr8Z_PVlCCdJ9GK_k_gf5bTcSk130_provenance.