Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_assertion description "[high levels of sCD30 in the common variable immunodeficiency patients with splenomegaly and the presence of lymphoma in a patient with the highest level of sCD30 may suggest a soluble form of this marker as a prognostic tool in such diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_assertion evidence source_evidence_literature NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_assertion SIO_000772 17912490 NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_assertion wasDerivedFrom lhgdn-20090331 NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_assertion wasGeneratedBy ECO_0000203 NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP229856.RAzcR05xDh60m_avXkF32L2E1zxgYHuHN23TbvYps1-VU130_provenance.