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- source_evidence_literature type ECO_0000212 NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_assertion wasGeneratedBy ECO_0000203 NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_assertion wasDerivedFrom befree-20150227 NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_assertion SIO_000772 24344182 NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_assertion evidence source_evidence_literature NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.
- NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_assertion description "[Septin 9 (SEPT9) interacts with microtubules (MTs) and is mutated in hereditary neuralgic amyotrophy (HNA), an autosomal-dominant neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853192.RAH95El9ydu-ZwXtZ7rh8_CafA3e2_AvzEEzmYgR8pawo130_provenance.