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- source_evidence_literature type ECO_0000212 NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_assertion description "[Most mutations in the myelin protein zero gene (MPZ) typically cause a severe demyelinating/dysmyelinating neuropathy that begins in infancy or an adult-onset axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_assertion evidence source_evidence_literature NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_assertion SIO_000772 17172621 NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_assertion wasDerivedFrom befree-2016 NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_assertion wasGeneratedBy ECO_0000203 NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.
- befree-2016 importedOn "2016-02-19" NP584535.RA1m6z6V2gtMbKFoXEryf8oScA81Sfu2ZGyaeL8sbkvOA130_provenance.