Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion> ?p ?o ?g. }
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- NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion type Assertion NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_head.
- NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion description "[In man, mutations in the NMD factor gene UPF3B, which disrupts a branch of the NMD pathway, cause various forms of intellectual disability (ID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion evidence source_evidence_literature NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion SIO_000772 22182939 NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion wasDerivedFrom befree-20140225 NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_assertion wasGeneratedBy ECO_0000203 NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.