Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion> ?p ?o ?g. }
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- NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_assertion type Assertion NP1406127.RA2oLXrQhJNw2C3dq6eSX6SYkFuVlH1RfNCmemcKL3lvI130_head.
- 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.