Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_assertion description "[Cerebellar malformations consistent with the MTS may be relatively common in patients with juvenile NPHP without classic symptoms of JS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_assertion evidence source_evidence_literature NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_assertion SIO_000772 15138899 NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_assertion wasDerivedFrom befree-20150227 NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_assertion wasGeneratedBy ECO_0000203 NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP792644.RA88lOB55OE5IAU44IE4WmS1pSzwt3Ne0a0B_0mH3C-0A130_provenance.