Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_assertion description "[Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_assertion evidence source_evidence_literature NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_assertion SIO_000772 7704558 NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_assertion wasDerivedFrom befree-20150227 NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_assertion wasGeneratedBy ECO_0000203 NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP667243.RA_ahsFdUG_VXWaqgwSZvXq6rjPo6N3p2z84uQP6yX06M130_provenance.