Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_assertion evidence source_evidence_literature NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_assertion SIO_000772 20645406 NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_assertion wasDerivedFrom befree-2016 NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_assertion wasGeneratedBy ECO_0000203 NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- befree-2016 importedOn "2016-02-19" NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.