Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_assertion description "[The ZRS contains point mutations that segregate with polydactyly in four unrelated families with PPD and in the Hx mouse mutant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_assertion evidence source_evidence_literature NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_assertion SIO_000772 12837695 NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_assertion wasDerivedFrom befree-2016 NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_assertion wasGeneratedBy ECO_0000203 NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.
- befree-2016 importedOn "2016-02-19" NP400150.RADxYgqbkLk1tISx6gOfekAPZHYO-SYkS79t16OfrJvIc130_provenance.