Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_assertion description "[Among them, ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) syndrome is caused by single point mutations in the p63 gene, which controls epidermal development and homeostasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_assertion evidence source_evidence_literature NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_assertion SIO_000772 23355677 NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_assertion wasDerivedFrom befree-20150227 NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_assertion wasGeneratedBy ECO_0000203 NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674802.RACMgnqNq2VG4P_QiW6SHdG91JA3vsgIoJlIJZQGe-xi0130_provenance.