Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_assertion wasGeneratedBy ECO_0000203 NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_assertion wasDerivedFrom befree-20150227 NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_assertion SIO_000772 17224651 NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_assertion evidence source_evidence_literature NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.
- NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_assertion description "[Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799667.RAA5zRvQZuUIoTALlN5UzD-BwvRMbteTVx03TTilsXYRk130_provenance.