Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- befree-2016 importedOn "2016-02-19" NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_assertion wasGeneratedBy ECO_0000203 NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_assertion wasDerivedFrom befree-2016 NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_assertion SIO_000772 25146893 NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_assertion evidence source_evidence_literature NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.
- NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_assertion description "[Loss of function mutations in TSHR, PAX8, NKX2.1, NKX2.5 and FOXE1 genes are responsible for some forms of inherited congenital hypothyroidism, with or without hypoplastic thyroid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1212722.RAi6qWjrZvJrw-w2vS8_wBm8eiLc-RPzt8hKEetsBStck130_provenance.