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- NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_assertion type Assertion NP217042.RAD7GPNHfKgATdWyrg7OQV7t0dHqZ9eEKFkNiyrQvKno8130_head.
- 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.