Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_assertion description "[G6PD deficiency results from many different point mutations in the X-linked gene encoding G6PD and is the most common human enzymopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_assertion evidence source_evidence_literature NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_assertion SIO_000772 10745013 NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_assertion wasDerivedFrom befree-20140225 NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_assertion wasGeneratedBy ECO_0000203 NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.
- befree-20140225 importedOn "2014-02-25" NP503949.RA_1D4FoWuDbFXbTV4lrx0DS4FhFD11kRz6HljK6Chf64130_provenance.