Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_assertion description "[Mutations in the gene encoding the TFAP2B transcription factor can cause Char syndrome with cardiac, craniofacial, and hand abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_assertion evidence source_evidence_literature NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_assertion SIO_000772 18752453 NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_assertion wasDerivedFrom befree-2016 NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_assertion wasGeneratedBy ECO_0000203 NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.
- befree-2016 importedOn "2016-02-19" NP690063.RAyeEdUrdznrJRcK2kQ78BtsZGa6pNOqDWXThfR5LC4wU130_provenance.