Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_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." NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_assertion evidence source_evidence_literature NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_assertion SIO_000772 12542510 NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_assertion wasDerivedFrom befree-2016 NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_assertion wasGeneratedBy ECO_0000203 NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.
- befree-2016 importedOn "2016-02-19" NP381106.RAmNa3OZWzwJZBd-oOvW-6x900-FVJrqWgNeBwYljKTkA130_provenance.