Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_assertion evidence source_evidence_literature NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_assertion SIO_000772 19293842 NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_assertion wasDerivedFrom gad-20150221 NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_assertion wasGeneratedBy ECO_0000203 NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.
- gad-20150221 importedOn "2015-02-21" NP68210.RAbyUUoH6hyXNX6LhyOqzp-prws-sNjuZlhpg0ZlZAZ3o130_provenance.