Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- befree-2016 importedOn "2016-02-19" NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_assertion wasGeneratedBy ECO_0000203 NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_assertion wasDerivedFrom befree-2016 NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_assertion SIO_000772 11556849 NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_assertion evidence source_evidence_literature NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.
- NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_assertion description "[Children with SNHL or MHL should be tested for Cx26 mutations early in their evaluation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330168.RA_6VfvSAuvfA9-K9EdAdW-tY8OS9OR-B4jMEw-DaL__4130_provenance.