Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_assertion description "[The discovery that Jak3 mutations are a significant cause of severe combined immunodeficiency (SCID), a rare inherited defect characterized by lymphopenia, has provided valuable insights into the functions of Jak3 in lymphoid development and function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_assertion evidence source_evidence_literature NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_assertion SIO_000772 15220007 NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_assertion wasDerivedFrom befree-20150227 NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_assertion wasGeneratedBy ECO_0000203 NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP519862.RAKSwSJWlj3I_81nX9axeizBvkLtUz_FiElYTvPNifrFQ130_provenance.