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- NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_assertion type Assertion NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_head.
- NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_assertion description "[We identified mutations of the SH2D1A gene only in the majority of patients presenting with fatal mononucleosis or an XLP family history, but not in any of the other patients studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_provenance.
- NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_assertion evidence source_evidence_literature NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_provenance.
- NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_assertion SIO_000772 12224001 NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_provenance.
- NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_assertion wasDerivedFrom befree-20150227 NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_provenance.
- NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_assertion wasGeneratedBy ECO_0000203 NP541887.RAZANM5bDTlQ8zSi0-U-4xHKLnF46q2r31Bo3prgEJKu0130_provenance.