Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_assertion description "[Additional clinical features were noted, including optic atrophy and ataxia for patients with SPG5 and ataxia and a chronic progressive external ophthalmoplegia-like phenotype for SPG7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_assertion evidence source_evidence_literature NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_assertion SIO_000772 23812641 NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_assertion wasDerivedFrom befree-20150227 NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_assertion wasGeneratedBy ECO_0000203 NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710132.RAQAGabi6Pdj6RwCCdUPZGzmSCtIAgz0TAO0XcBZPcxds130_provenance.