Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_assertion description "[Low-resolution genotyping of HLA-A, HLA-B, and HLA-DR loci and genotyping of TNFA -238A/G and TNFA -308A/G single-nucleotide polymorphisms were performed in 48 consecutive CSS patients and 350 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_assertion evidence source_evidence_literature NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_assertion SIO_000772 17763415 NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_assertion wasDerivedFrom gad-20150221 NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_assertion wasGeneratedBy ECO_0000203 NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP138897.RAI2QzCdgLMFdM4hei0Pq35OjKmPLwRohMO2WESKt_HJ0130_provenance.