Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_assertion description "[Mutations in the HNF1B gene have been shown to cause renal malformations, hypomagnesemia, and MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_assertion evidence source_evidence_literature NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_assertion SIO_000772 24204001 NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_assertion wasDerivedFrom befree-2016 NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_assertion wasGeneratedBy ECO_0000203 NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1126013.RA47XUTE9KvK3rxR-hE0fiqzlYlmind-cA7VXqRxIXgqE130_provenance.