Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion> ?p ?o ?g. }
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- NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion type Assertion NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_head.
- NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion wasGeneratedBy ECO_0000203 NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_provenance.
- NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion wasDerivedFrom befree-20140225 NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_provenance.
- NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion SIO_000772 22069374 NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_provenance.
- NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion evidence source_evidence_literature NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_provenance.
- NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_assertion description "[X-linked lymphoproliferative disease (XLP) is a primary immunodeficiency caused by mutations in SH2D1A which encodes SAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692467.RAUeE9dU-I6aVJSzLeel9fr8CdBTEwblxmqF0JvIVg4qw130_provenance.