Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP515427.RAlK-piyGHqmQNIB9mQvxQDNiVHqJNbvIpINPzxFtK8Zo130_provenance.