Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_assertion description "[We conclude that molecular diagnosis is a necessary adjunct for clinical diagnosis and management of inherited and sporadic neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_assertion evidence source_evidence_literature NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_assertion SIO_000772 11835375 NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_assertion wasDerivedFrom gad-20130706 NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_assertion wasGeneratedBy ECO_0000203 NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP53940.RAJGn4tLHL-1xrFdUJYBstio_0xE8k3GjHMlqtJeLPRUQ130_provenance.