Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_assertion description "[A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_assertion evidence source_evidence_literature NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_assertion SIO_000772 16688595 NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_assertion wasDerivedFrom befree-2016 NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_assertion wasGeneratedBy ECO_0000203 NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.
- befree-2016 importedOn "2016-02-19" NP549208.RAeQIqEquO00PsXj0QUe5NewoYSr2MZaKu7MhnWVR-XwY130_provenance.