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- source_evidence_literature type ECO_0000212 NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_assertion description "[report that an autosomal recessive infantile parkinsonism-dystonia is caused by loss-of-function mutations in DAT that impair dopamine reuptake (see the related article beginning on page 1595).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_assertion evidence source_evidence_literature NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_assertion SIO_000772 19504720 NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_assertion wasDerivedFrom befree-2016 NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_assertion wasGeneratedBy ECO_0000203 NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.
- befree-2016 importedOn "2016-02-19" NP743704.RAo917qCP_6QQ52dJmIcdHCF7jmeof1pAJ36mblgXmNPI130_provenance.