Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_assertion wasGeneratedBy ECO_0000203 NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_assertion wasDerivedFrom befree-20140225 NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_assertion SIO_000772 20718765 NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_assertion evidence source_evidence_literature NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_assertion description "[The PAX8 gene was sequenced in a mother and child both suffering from congenital hypothyroidism (CH) because of thyroid hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP305915.RA1T72ZdOHB853ywaZFhK_jmgLShgtfkq-H0XpA8ZsC4U130_provenance.