Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_assertion description "[PANK2 mutations are associated with all cases of classic Hallervorden-Spatz syndrome and one third of cases of atypical disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_assertion evidence source_evidence_literature NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_assertion SIO_000772 12510040 NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_assertion wasDerivedFrom befree-20140225 NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_assertion wasGeneratedBy ECO_0000203 NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_provenance.