Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion> ?p ?o ?g. }
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- NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion type Assertion NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_head.
- NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion description "[Mutations in GJB1, the gene for connexin 32 (Cx32) cause the second most common form of Charcot-Marie-Tooth disease (CMT1X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_provenance.
- NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion evidence source_evidence_literature NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_provenance.
- NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion SIO_000772 21871435 NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_provenance.
- NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion wasDerivedFrom befree-20150227 NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_provenance.
- NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_assertion wasGeneratedBy ECO_0000203 NP426046.RAIVJOuHddz9uAAoeeNTNp4XK2J8ruLfQhdcQz7NzwAXs130_provenance.