Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_assertion description "[The most frequent p63 mutation syndrome is the EEC syndrome, characterized by ectrodactyly, ectodermal dysplasia and cleft lip/palate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_assertion evidence source_evidence_literature NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_assertion SIO_000772 23407076 NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_assertion wasDerivedFrom befree-2016 NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_assertion wasGeneratedBy ECO_0000203 NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1052823.RAZPo0YJNzuvM39GBBZ0zSqFEA3V43UxncM1OooaQqTqI130_provenance.