Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_assertion description "[On analysis of common genetic variants of HspA1L, HspA1A and HspA1B, a haplotype significantly associated with SLE in the Erlangen-SLE cohort was identified, which was confirmed in the OMRF cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_assertion evidence source_evidence_literature NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_assertion SIO_000772 20498198 NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_assertion wasDerivedFrom befree-20140225 NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_assertion wasGeneratedBy ECO_0000203 NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806808.RAB3GP9pxN_imiIh-sq8ycg6ZGh3c_OV4-St8s_5Q3mFk130_provenance.