Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion> ?p ?o ?g. }
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- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion type Assertion NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_head.
- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion description "[Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion evidence source_evidence_literature NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion SIO_000772 15660919 NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion wasDerivedFrom befree-20140225 NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_assertion wasGeneratedBy ECO_0000203 NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.