Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_assertion description "[Mutations of the tumour-suppressor gene NF1 (neurofibromatosis 1) have been observed in neurofibromas and neurofibrosarcomas of patients with von Recklinghausen's disease and in sporadic nerve sheath tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_assertion evidence source_evidence_literature NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_assertion SIO_000772 11129335 NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_assertion wasDerivedFrom befree-2016 NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_assertion wasGeneratedBy ECO_0000203 NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP303809.RApw2ryMm7Nm7vhO79JRdGxbaS5lTPeXxU28bbm8DoRqQ130_provenance.