Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_assertion description "[A case of atypical hemolytic uremic syndrome due to anti-factor H antibody in a patient presenting with a factor XII deficiency identified two novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_assertion evidence source_evidence_literature NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_assertion SIO_000772 21271273 NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_assertion wasDerivedFrom befree-2016 NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_assertion wasGeneratedBy ECO_0000203 NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.
- befree-2016 importedOn "2016-02-19" NP868146.RAxz73wUDHHM5AwPJCLuF05G3Ka-bscZwakSJLCYUYUyU130_provenance.