Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_assertion description "[These findings suggest that the AC and SCC subtypes may arise from a common cell of origin and they are driven to their distinct phenotypic end points by altered expression of a limited number of key genes such as p63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_assertion evidence source_evidence_literature NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_assertion SIO_000772 16869734 NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_assertion wasDerivedFrom befree-2016 NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_assertion wasGeneratedBy ECO_0000203 NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.
- befree-2016 importedOn "2016-02-19" NP561486.RA2r0Gi4ZCuH5bv1dm-yUlq0Xe4zidwQeRnhXh6Ae133w130_provenance.