Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_assertion> ?p ?o ?g. }
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- NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_assertion type Assertion NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_head.
- NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_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." NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_assertion evidence source_evidence_literature NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_assertion SIO_000772 12224001 NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_assertion wasDerivedFrom befree-20140225 NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_assertion wasGeneratedBy ECO_0000203 NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.