Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_assertion description "[We conclude that the presence of 1 or 2 C4A null allotypes and the presence of a C4A gene deletion identify subgroups of patients with SLE that differ in clinical, laboratory, and autoantibody characteristics from other patients with SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_assertion evidence source_evidence_literature NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_assertion SIO_000772 8341140 NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_assertion wasDerivedFrom befree-20150227 NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_assertion wasGeneratedBy ECO_0000203 NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013665.RAmx-XliMqT4yhatLOKyJ9IwHzFx3HWj-pBaGvdqjFiU8130_provenance.