Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_assertion description "[Detailed analysis of the different PMP22 mutants revealed, in addition to the obvious myelinopathy, distal axonopathy as a characteristic feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_assertion evidence source_evidence_literature NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_assertion SIO_000772 10586249 NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_assertion wasDerivedFrom befree-2016 NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_assertion wasGeneratedBy ECO_0000203 NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.
- befree-2016 importedOn "2016-02-19" NP269206.RA8WK91OkAIYV5cBtHR1Q9EU9Mpcr62_YPKvSOqe3I_Ko130_provenance.