Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_assertion description "[Our finding expands the spectrum of cataract phenotypes caused by the Q155X mutation of CRYBB2, confirms the phenotypic heterogeneity of this mutation and suggests the mechanism that influences the congenital cataract formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_assertion evidence source_evidence_literature NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_assertion SIO_000772 16179907 NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_assertion wasDerivedFrom lhgdn-20090331 NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_assertion wasGeneratedBy ECO_0000203 NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198493.RAtm140jvqw9demj7tgTbruN-OI7oaiqLhWXss_VnF1Ag130_provenance.