Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- befree-2016 importedOn "2016-02-19" NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_assertion wasGeneratedBy ECO_0000203 NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_assertion wasDerivedFrom befree-2016 NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_assertion SIO_000772 12734540 NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_assertion evidence source_evidence_literature NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.
- NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_assertion description "[Germline mutations in the RET proto-oncogene are responsible for the development of human hereditary diseases, including multiple endocrine neoplasia (MEN) type 2A and 2B, familial medullary thyroid carcinoma (FMTC), and Hirschsprung's disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393447.RAwRuH_5H3JSNnfnYYXN37bWrINrHVuUYUhOiFWRZDxpg130_provenance.