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- source_evidence_literature type ECO_0000212 NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_assertion description "[Mutations in FA2H are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_assertion evidence source_evidence_literature NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_assertion SIO_000772 19068277 NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_assertion wasDerivedFrom lhgdn-20090331 NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_assertion wasGeneratedBy ECO_0000203 NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP203905.RAAh3k3Fwqm_jsmxo1ILABF9DPyPBh_0XyYZ1F-uWqSjY130_provenance.