Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_assertion description "[In the process of screening the above cohort of patients as well as other patients for CMT-causative mutations, we identified several previously unreported mutant alleles: two for connexin 32, three for myelin protein zero, and two for peripheral myelin protein 22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_assertion evidence source_evidence_literature NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_assertion SIO_000772 11835375 NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_assertion wasDerivedFrom gad-20150221 NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_assertion wasGeneratedBy ECO_0000203 NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP68206.RAtjpi2JnN_n95xUkodxZO-0mq5iXkmsx9Oy32rmDLDG0130_provenance.