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- source_evidence_literature type ECO_0000212 NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_assertion evidence source_evidence_literature NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_assertion SIO_000772 22998673 NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_assertion wasDerivedFrom befree-20150227 NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_assertion wasGeneratedBy ECO_0000203 NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719402.RAYiF_6Ery2eWVHmRu5G79VmBpafrPTyEC2XboFeyW9uk130_provenance.