Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_assertion description "[Having explained the digital findings and macrocephaly, the skeletal changes were thought to fit best congenital spondyloepiphyseal dysplasia (SEDC MIM #183900), a type II collagen disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_assertion evidence source_evidence_literature NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_assertion SIO_000772 10678662 NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_assertion wasDerivedFrom befree-2016 NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_assertion wasGeneratedBy ECO_0000203 NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.
- befree-2016 importedOn "2016-02-19" NP275332.RAr7vpQZGg8sIFt8IKL2aS7wBS276L1bXIJ6NSfJysmmU130_provenance.