Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion> ?p ?o ?g. }
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- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion type Assertion NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_head.
- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion description "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_provenance.
- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion evidence source_evidence_literature NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_provenance.
- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion SIO_000772 18379723 NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_provenance.
- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion wasDerivedFrom befree-20140225 NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_provenance.
- NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_assertion wasGeneratedBy ECO_0000203 NP366720.RAH_BreexoKK6iMyKTjh_8OWKHW0FRLFuUdKEmah_R0AQ130_provenance.