Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_assertion description "[Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_assertion evidence source_evidence_curated NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_assertion SIO_000772 11438991 NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_assertion wasDerivedFrom uniprot-2016 NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_assertion wasGeneratedBy ECO_0000218 NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1496.RAuwslggmF-pho0brpgicrF0_HEKB7OTAx16rTml0SdSQ130_provenance.