Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_assertion description "[CMT2 is an axonal neuropathy of undetermined cause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_assertion evidence source_evidence_literature NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_assertion SIO_000772 7804455 NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_assertion wasDerivedFrom befree-20140225 NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_assertion wasGeneratedBy ECO_0000203 NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP678318.RATWxIp46v9CUZDcrKzgf8PwQhLzFADUZuqpOdEmK5sv0130_provenance.