Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_assertion description "[The desmuslin gene was screened for mutations in 71 patients with various forms of myopathy for which there was no known cause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_assertion evidence source_evidence_literature NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_assertion SIO_000772 11454237 NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_assertion wasDerivedFrom befree-2016 NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_assertion wasGeneratedBy ECO_0000203 NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.
- befree-2016 importedOn "2016-02-19" NP323892.RADPdlnRkcFKaL__rVdJjWlDfVBpwqehgfswd4Qh8fNNc130_provenance.