Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_assertion wasGeneratedBy ECO_0000203 NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_assertion wasDerivedFrom befree-20150227 NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_assertion SIO_000772 8988167 NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_assertion evidence source_evidence_literature NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.
- NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_assertion description "[Saethre-Chotzen syndrome (acrocephalo-syndactyly type III, ACS III) is an autosomal dominant craniosynostosis with brachydactyly, soft tissue syndactyly and facial dysmorphism including ptosis, facial asymmetry and prominent ear crura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762143.RAdxg6w1924O6mp7yaK2DIHeZaWuH_hrf8Kt7KXxFdcfE130_provenance.