Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_assertion wasGeneratedBy ECO_0000203 NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_assertion wasDerivedFrom befree-20140225 NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_assertion SIO_000772 20584796 NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_assertion evidence source_evidence_literature NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP277863.RAcSS-hSaxXEpRBWNBm4Fge8X3_qJl_pj5DEYamd7nTUo130_provenance.