Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_assertion description "[To study whether the clinical manifestation of XLP gene defects and/or polymorphisms extends beyond the classically recognized phenotype, we analyzed patients for the presence of SH2D1A gene alterations who presented with fatal or nonfatal, yet unusually severe or chronic EBV infections, and other possibly EBV-associated diseases, such as Hodgkin's lymphomas or nonendemic Burkitt's lymphomas and Burkitt-type leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_assertion evidence source_evidence_literature NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_assertion SIO_000772 12224001 NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_assertion wasDerivedFrom befree-20150227 NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_assertion wasGeneratedBy ECO_0000203 NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541896.RAxBMhf_rFL1vkT4J43dMBWZvPZ4l_qleVl0OjRI9C4ZM130_provenance.