Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_assertion description "[A 7-year-old boy with dysmorphic features was found to have a recombinant chromosome 18, rec(18), resulting from meiotic recombination of a maternal pericentric inversion, inv(18) (p11.2q21.3), as defined by high-resolution banding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_assertion evidence source_evidence_literature NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_assertion SIO_000772 1753439 NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_assertion wasDerivedFrom befree-20140225 NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_assertion wasGeneratedBy ECO_0000203 NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP545911.RAdsQ_EP8ZISjU1cwjjKiE7C4NIpc8YsYOjd9JNBElJHM130_provenance.