Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_assertion description "[CMT1A and HNPP are apparent reciprocal duplication/deletion syndromes originating from unequal cross-over during germ-cell meiosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_assertion evidence source_evidence_literature NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_assertion SIO_000772 7952853 NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_assertion wasDerivedFrom befree-2016 NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_assertion wasGeneratedBy ECO_0000203 NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1328093.RAO-r4jSWiVp3gktS3HFMwZVAxlmR0tA1_MzUhN5-OgRw130_provenance.