Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion> ?p ?o ?g. }
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- NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion type Assertion NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_head.
- NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion description "[Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_provenance.
- NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion evidence source_evidence_literature NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_provenance.
- NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion SIO_000772 20170900 NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_provenance.
- NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion wasDerivedFrom befree-2016 NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_provenance.
- NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_assertion wasGeneratedBy ECO_0000203 NP794840.RAH8zAHpLlc-O9WX6vtkMwowEXnKYmAkIiEvnYIRJg3-c130_provenance.