Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_assertion description "[Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_assertion evidence source_evidence_literature NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_assertion SIO_000772 7927327 NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_assertion wasDerivedFrom befree-20150227 NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_assertion wasGeneratedBy ECO_0000203 NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP667245.RAp7LRCNqu3O_1aFqRoM0UgfrJzHmlDYwC7HX0ZGolPpE130_provenance.