Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion> ?p ?o ?g. }
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- NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion type Assertion NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_head.
- NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion description "[Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_provenance.
- NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion evidence source_evidence_literature NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_provenance.
- NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion SIO_000772 25480037 NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_provenance.
- NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion wasDerivedFrom befree-2016 NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_provenance.
- NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_assertion wasGeneratedBy ECO_0000203 NP1245284.RAq0ndU27dJm10O2d4tkSFFE6_ACEB-0gybcvNtKZRyt8130_provenance.