Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_assertion description "[The gene responsible for XLP has been identified as SH2D1A/DSHP/SLAM-associated protein (SAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_assertion evidence source_evidence_literature NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_assertion SIO_000772 15682426 NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_assertion wasDerivedFrom befree-2016 NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_assertion wasGeneratedBy ECO_0000203 NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.
- befree-2016 importedOn "2016-02-19" NP478661.RARIYkKp7vhDsbAKiHiTEbH2zjn1NEmMIm2UTuK1AlsuU130_provenance.