Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_assertion description "[Charcot-Marie-Tooth disease (CMT) is a genetically heterogeneous disorder that has been associated with alterations of several proteins: peripheral myelin protein 22, myelin protein zero, connexin 32, early growth response factor 2, periaxin, myotubularin related protein 2, N-myc downstream regulated gene 1 product, neurofilament light chain, and kinesin 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_assertion evidence source_evidence_literature NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_assertion SIO_000772 11835375 NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_assertion wasDerivedFrom gad-20130706 NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_assertion wasGeneratedBy ECO_0000203 NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.
- gad-20130706 importedOn "2013-07-06" NP53059.RALlTEHrfrj1yF213FCJqiJ5MDtq32feRneNAiSgg8o5A130_provenance.