Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP803148.RAr__3fv5bDli93P5aA0DmqBYw5eigtRsgoFfJMdEfxdc130_provenance.