Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_assertion description "[CMT1A and HNPP are apparent reciprocal duplication/deletion syndromes originating from unequal crossover during germ cell meiosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_assertion evidence source_evidence_literature NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_assertion SIO_000772 7849745 NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_assertion wasDerivedFrom befree-2016 NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_assertion wasGeneratedBy ECO_0000203 NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.
- befree-2016 importedOn "2016-02-19" NP1323777.RAzEMg0NCJt38lT7jEl27_RMvm4OjB_a8BRD_XYLei0ng130_provenance.