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- source_evidence_literature type ECO_0000212 NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_assertion description "[PKD1 is the most common site for mutations in human autosomal dominant polycystic kidney disease (ADPKD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_assertion evidence source_evidence_literature NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_assertion SIO_000772 9326937 NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_assertion wasDerivedFrom befree-2016 NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_assertion wasGeneratedBy ECO_0000203 NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1381731.RAo_Qyeor_5n-FZ2k96Sn49wIjWpPvVoFG5wZsozdNiCE130_provenance.