Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_assertion evidence source_evidence_literature NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_assertion SIO_000772 19068278 NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_assertion wasDerivedFrom befree-20150227 NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_assertion wasGeneratedBy ECO_0000203 NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724204.RA2VGP1BFXneQNHoSxi8G3pAxyLYKTHReGll52FzVwC_U130_provenance.