Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_assertion description "[Two siblings with deletion of the entire GJB1 gene had mild to moderate lower extremity muscle weakness and sensory disturbance without CNS involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_assertion evidence source_evidence_literature NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_assertion SIO_000772 12542510 NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_assertion wasDerivedFrom befree-20150227 NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_assertion wasGeneratedBy ECO_0000203 NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426184.RAkC2H-oL3NlgKtmiIE8at-NgxztCbQtv6ctr_kxdpHyg130_provenance.