Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_assertion description "[Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_assertion evidence source_evidence_literature NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_assertion SIO_000772 16282976 NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_assertion wasDerivedFrom befree-20140225 NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_assertion wasGeneratedBy ECO_0000203 NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP308630.RAonFqLRce2ljLNSGiF5fYDa7C18Z7BtNkSa1bCrWjLIs130_provenance.