Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_assertion wasGeneratedBy ECO_0000203 NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_assertion wasDerivedFrom befree-20150227 NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_assertion SIO_000772 19239083 NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_assertion evidence source_evidence_literature NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.
- NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_assertion description "[The ankyloblepharon-ectodermal defects-cleft lip and palate (Hay-Wells or AEC) and the Rapp-Hodgkin syndrome (RHS) are rare autosomal dominant ectodermal dysplasias due to mutations in the transcription factor gene P63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857019.RAhVDC-pF56g3UFc0DEnvGR0lL3lyAHnTa1_Dv2V91Omg130_provenance.