Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_assertion description "[The results provide novel mutations and copy number aberrations of CASK, causing MR with MICPCH, and also demonstrate the similarity of the phenotypes of MR with MICPCH regardless of the CASK mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_assertion evidence source_evidence_literature NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_assertion SIO_000772 21735175 NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_assertion wasDerivedFrom befree-2016 NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_assertion wasGeneratedBy ECO_0000203 NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.
- befree-2016 importedOn "2016-02-19" NP907680.RAnv0p5tYPQnaseaALfiGIKL5Q2sPpMkIMJNw-lmGIXBs130_provenance.