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- source_evidence_literature type ECO_0000212 NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_assertion evidence source_evidence_literature NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_assertion SIO_000772 18765513 NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_assertion wasDerivedFrom befree-20150227 NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_assertion wasGeneratedBy ECO_0000203 NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP897346.RANr4c6JHL3n9gEN5YQ_YuU1Ex75frrmreksQxMjilIXE130_provenance.