Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_assertion description "[These findings, combined with a Dock6 expression profile that is consistent with an AOS phenotype as well as the very recent demonstration of dominant mutations of ARHGAP31 in AOS, establish Cdc42 and Rac1 as key molecules in the pathogenesis of AOS and suggest that other regulators of these Rho GTPase proteins might be good candidates in the quest to define the genetic spectrum of this genetically heterogeneous condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_assertion evidence source_evidence_literature NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_assertion SIO_000772 21820096 NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_assertion wasDerivedFrom befree-2016 NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_assertion wasGeneratedBy ECO_0000203 NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.
- befree-2016 importedOn "2016-02-19" NP915051.RA1WRRKUldhPn_nPPio3KhG-EIY8S3LF91T3OtNs3u7ro130_provenance.