Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_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." NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_assertion evidence source_evidence_literature NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_assertion SIO_000772 11129335 NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_assertion wasDerivedFrom befree-2016 NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_assertion wasGeneratedBy ECO_0000203 NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.
- befree-2016 importedOn "2016-02-19" NP303811.RAvZdE3Epa_QfLo0qu0f5cJq1MCQuqtS6Lj9LS-hNTdPs130_provenance.