Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_assertion description "[Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_assertion evidence source_evidence_literature NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_assertion SIO_000772 18953341 NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_assertion wasDerivedFrom befree-20140225 NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_assertion wasGeneratedBy ECO_0000203 NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP314382.RA3maIwiCxZmYrK8WwSehBdIYIN41lMcUeWgThSe7atXk130_provenance.