Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_assertion> ?p ?o ?g. }
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- NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_assertion type Assertion NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_head.
- NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_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." NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_provenance.
- NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_assertion evidence source_evidence_literature NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_provenance.
- NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_assertion SIO_000772 12224001 NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_provenance.
- NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_assertion wasDerivedFrom befree-20140225 NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_provenance.
- NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_assertion wasGeneratedBy ECO_0000203 NP184475.RA-vjdxSfOSTThe9j6J3mOIepBlFoNnUVe-Gy-rik-KQw130_provenance.