Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_assertion description "[BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_assertion evidence source_evidence_literature NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_assertion SIO_000772 12016587 NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_assertion wasDerivedFrom befree-20150227 NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_assertion wasGeneratedBy ECO_0000203 NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP259781.RANlBh9HA48tCbldDIN8i_WZBOAw6LcbtFSk_sa5F2BgE130_provenance.