Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_assertion description "[The patient is examined in light of other reported patients with deletions and/or translocations involving the regions between 11p12 --> 11p14 including patients with WAGR + obesity (WAGRO) as well as with other reported patients with aniridia and congenital ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_assertion evidence source_evidence_literature NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_assertion SIO_000772 16646034 NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_assertion wasDerivedFrom befree-20150227 NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_assertion wasGeneratedBy ECO_0000203 NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778086.RAxAlSYnAe0g1ddO0YXQSFBjhn-0My4lu8-m-7SjpSxuM130_provenance.