Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_assertion wasGeneratedBy ECO_0000203 NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_assertion wasDerivedFrom befree-2016 NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_assertion SIO_000772 8675603 NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_assertion evidence source_evidence_literature NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.
- NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_assertion description "[The cosegregation of multiple endocrine neoplasia (MEN) type 2A with Hirschsprung's disease (HSCR), two diseases associated with mutation of the RET proto-oncogene, is infrequent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1352488.RASiP20XGT7vFk_Mf07g4J9H5e0jeWfjgwXHjMNZ_JyYk130_provenance.