Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_assertion description "[We report a new point mutation in the p63 gene in a family in which the mother was initially diagnosed with Rapp-Hodgkin syndrome and her two offspring manifested ankyloblepharon, ectodermal defects, cleft lip and palate, syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_assertion evidence source_evidence_literature NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_assertion SIO_000772 16190990 NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_assertion wasDerivedFrom befree-20150227 NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_assertion wasGeneratedBy ECO_0000203 NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP799872.RAHAom1WkqgFpkEE3U86cNhVk67nBslaQXr7K8MwWEbdA130_provenance.