Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_assertion description "[Myelin protein zero (MPZ) mutations cause demyelinating neuropathies that range from severe neonatal to milder adult forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_assertion evidence source_evidence_literature NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_assertion SIO_000772 17602703 NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_assertion wasDerivedFrom befree-20150227 NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_assertion wasGeneratedBy ECO_0000203 NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568271.RAaeqsOWV8WdUcohnW0JNKmZN0uPF4CAFOiK3-NGP6j1o130_provenance.