Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_assertion description "[When the mutation is located on chromosome 16 (PKD1), extra-renal manifestations such as the rupture of intracranial aneurysms are well known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_assertion evidence source_evidence_literature NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_assertion SIO_000772 8749697 NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_assertion wasDerivedFrom befree-20140225 NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_assertion wasGeneratedBy ECO_0000203 NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP731605.RAofnzYP1nMq_bwm1suQy0ddOw-EtiEI4ADuhP9c2Uj3M130_provenance.