Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_assertion description "[DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_assertion evidence source_evidence_literature NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_assertion SIO_000772 2896160 NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_assertion wasDerivedFrom befree-20140225 NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_assertion wasGeneratedBy ECO_0000203 NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP215572.RALDJqIMFs3SyEh9xl5nrr3ieAA4yH286gs2VHYQ2vAS8130_provenance.