Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion description "[Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion evidence source_evidence_literature NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion SIO_000772 9778454 NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion wasDerivedFrom befree-2016 NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion wasGeneratedBy ECO_0000203 NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_provenance.