Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_assertion description "[Testing for GTPCH deficiency should be considered for patients with unexplained neurological symptoms and extrapyramidal movement disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_assertion evidence source_evidence_literature NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_assertion SIO_000772 18276179 NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_assertion wasDerivedFrom befree-20150227 NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_assertion wasGeneratedBy ECO_0000203 NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP935626.RAWPKBPMet2ZI-YqwVVc1nOsZH6IZ0XEcErQt28e13-mY130_provenance.