Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_assertion description "[X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_assertion evidence source_evidence_literature NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_assertion SIO_000772 10219749 NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_assertion wasDerivedFrom befree-2016 NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_assertion wasGeneratedBy ECO_0000203 NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.
- befree-2016 importedOn "2016-02-19" NP251191.RAxqX_vC7wAY7jtvvzkB7LuDiJR9bpKY1A0mf8gWyhNl0130_provenance.