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- source_evidence_literature type ECO_0000212 NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_assertion description "[At present, the list of genes involved in human non-syndromic hypodontia includes not only those encoding a signaling molecule (TGFA) and transcription factors (MSX1 and PAX9) that play critical roles during early craniofacial development, but also genes coding for a protein involved in canonical Wnt signaling (AXIN2), and a transmembrane receptor of fibroblast growth factors (FGFR1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_assertion evidence source_evidence_literature NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_assertion SIO_000772 18771513 NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_assertion wasDerivedFrom befree-20150227 NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_assertion wasGeneratedBy ECO_0000203 NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP571697.RAQ-oC0AvCFTk-EHGHeVAjwqRbMLDZHiNzEtmxTv07uOI130_provenance.