Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP615177.RA4z76mX4ekJFJ6Q3DDaWwb4bn6ixX58PCzT-C_fYUYz8130_provenance.