Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_assertion description "[GLIS3 mutations in humans lead to neonatal diabetes, hypothyroidism, and cystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_assertion evidence source_evidence_literature NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_assertion SIO_000772 19481545 NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_assertion wasDerivedFrom befree-2016 NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_assertion wasGeneratedBy ECO_0000203 NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.
- befree-2016 importedOn "2016-02-19" NP741983.RA7F2vNuhs24E6W1gvl-ITn_V0PWHTA7KJXuJvPev5YvA130_provenance.