Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion> ?p ?o ?g. }
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- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion type Assertion NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_head.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion description "[Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion evidence source_evidence_literature NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion SIO_000772 11266688 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion wasDerivedFrom befree-2016 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.
- NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_assertion wasGeneratedBy ECO_0000203 NP312058.RAYVQ06wC1EGnzZ7jLmM5G80Vo3ObCTUSykjSgcfIPcoE130_provenance.