Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_assertion description "[Cx43 proteins containing ODDD mutations found in the N-terminus (Y17S), first transmembrane domain (G21R, A40V), second transmembrane domain (L90V), and cytoplasmic loop (I130T, K134E) do form gap junction plaques but show compromised channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_assertion evidence source_evidence_literature NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_assertion SIO_000772 15879313 NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_assertion wasDerivedFrom befree-2016 NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_assertion wasGeneratedBy ECO_0000203 NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP493628.RAA1q65zkrZFsYVnLGF5anNio1tQNVop0_QN4rJreefR0130_provenance.