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- source_evidence_literature type ECO_0000212 NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_assertion description "[Another candidate gene at 3q27, SOX2, was also considered because of its suspected role as a transcription factor in early development and because of known examples of SOX genes that are loci for dominantly inherited developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_assertion evidence source_evidence_literature NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_assertion SIO_000772 10480362 NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_assertion wasDerivedFrom befree-2016 NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_assertion wasGeneratedBy ECO_0000203 NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.
- befree-2016 importedOn "2016-02-19" NP262529.RAEaAsuGj3DKdMqX30ddf_lgH_e6bBEwxECEa4TyFsQkE130_provenance.