Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_assertion wasGeneratedBy ECO_0000203 NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_assertion wasDerivedFrom befree-20150227 NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_assertion SIO_000772 20718767 NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_assertion evidence source_evidence_literature NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.
- NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_assertion description "[Nonsyndromic autosomal recessively inherited nongoitrous congenital hypothyroidism (CHNG) can be caused by mutations in TSHR, PAX8, TSHB and NKX2-5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760438.RA2GfLCANhAqkPWZ0MnhoxhN8RpmE8Aw5xT9rGgxlxeQ0130_provenance.