Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_assertion description "[Mutations in myotubularin, amphiphysin 2 (BIN1), and dynamin 2 lead to different forms of centronuclear myopathy, while mutations in myotubularin-related proteins cause Charcot-Marie-Tooth neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_assertion evidence source_evidence_literature NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_assertion SIO_000772 22496665 NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_assertion wasDerivedFrom befree-2016 NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_assertion wasGeneratedBy ECO_0000203 NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.
- befree-2016 importedOn "2016-02-19" NP974358.RAeC2fjY6AIYqr-nIyxNwQU7oR9_PU2XXMXcKxmQyHFNA130_provenance.