Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_assertion description "[Pyrimidine 5' -nucleotidase (P5'N-1) deficiency is the third most common enzyme abnormality after glucose 6-phosphate dehydrogenase and pyruvate kinase causing hereditary non-spherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_assertion evidence source_evidence_literature NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_assertion SIO_000772 16522554 NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_assertion wasDerivedFrom befree-20140225 NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_assertion wasGeneratedBy ECO_0000203 NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718876.RAuvK-g31KXM4_LvSMFfM74cv6UqKgrB39QJ2_tIXNlwQ130_provenance.