Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_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." NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_assertion evidence source_evidence_literature NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_assertion SIO_000772 23407076 NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_assertion wasDerivedFrom befree-20150227 NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_assertion wasGeneratedBy ECO_0000203 NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP767891.RAxsr8vOx3oFb_Rhq5tfQDB0-iH9MJ6CWkhgewdYFXwtw130_provenance.