Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_assertion description "[Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal disease caused by inactivating germ-line mutations of HRPT2 gene, with subsequent loss of Parafibromin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_assertion evidence source_evidence_literature NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_assertion SIO_000772 19529956 NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_assertion wasDerivedFrom befree-20140225 NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_assertion wasGeneratedBy ECO_0000203 NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212253.RAAbhvcnkuxbrzwAAsjRkJD-FcqzIAxl4E6JhgkyrCn-A130_provenance.