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- source_evidence_literature type ECO_0000212 NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_assertion wasGeneratedBy ECO_0000203 NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_assertion wasDerivedFrom gad-20150221 NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_assertion SIO_000772 20687945 NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_assertion evidence source_evidence_literature NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.
- NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_assertion description "[Here, we describe a screening method, HRM, for the detection of both heterozygous and homozygous mutations in the gene encoding MUTYH in selected samples of patients with phenotype of MAP. We refine the capabilities of HRM-PCR and apply it to a gene not y]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91068.RAxnIoDGC8wZ46_sHoIg0yjpeaLcjzrPmkPyOb14zPG8A130_provenance.