Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion description "[To clarify the clinical phenotype and molecular mechanism in X-linked Charcot-Marie-Tooth disease (CMTX) patients with a deletion of the whole connexin 32 (Cx32) coding sequence, we studied a family with this deletion by electrophysiology, Southern blotting and quantitative PCR analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion evidence source_evidence_literature NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion SIO_000772 11266688 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion wasDerivedFrom befree-2016 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion wasGeneratedBy ECO_0000203 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- befree-2016 importedOn "2016-02-19" NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.