Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_assertion description "[GEP NETs occur either sporadically or as part of endocrine tumor susceptibility syndromes such as multiple endocrine neoplasia type 1 (MEN1), von Hippel Lindau (VHL) syndrome, neurofibromatosis (NF-1), and possibly tuberous sclerosis (TSC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_assertion evidence source_evidence_literature NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_assertion SIO_000772 19125015 NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_assertion wasDerivedFrom befree-20140225 NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_assertion wasGeneratedBy ECO_0000203 NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP402646.RAF3kXzUhXBfePvD7FYEYKdUL8io8UQJ_pPqdeSgkug_c130_provenance.