Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_assertion wasGeneratedBy ECO_0000203 NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_assertion wasDerivedFrom befree-20150227 NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_assertion SIO_000772 24344182 NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_assertion evidence source_evidence_literature NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.
- NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_assertion description "[SEPT9 isoforms lacking repeat motifs or containing the HNA-linked mutation R88W, which maps to the R/K-R-x-E motif, diminished intracellular MT bundling and impaired asymmetric neurite growth in PC-12 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853240.RAmU3uKeCA1O5pPuSRWJZyRIn2RZvv8ephSV6HVD-leZY130_provenance.