Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion description "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion evidence source_evidence_literature NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion SIO_000772 9595994 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion wasDerivedFrom befree-20140225 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion wasGeneratedBy ECO_0000203 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.