Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- befree-2016 importedOn "2016-02-19" NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_assertion wasGeneratedBy ECO_0000203 NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_assertion wasDerivedFrom befree-2016 NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_assertion SIO_000772 10978357 NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_assertion evidence source_evidence_literature NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_assertion description "[Mutations in RET and in two members of the GDNF ligand family are associated with Hirschsprung disease (HSCR), a congenital absence of the enteric ganglia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.