Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_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." NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_assertion evidence source_evidence_literature NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_assertion SIO_000772 10978357 NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_assertion wasDerivedFrom befree-2016 NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_assertion wasGeneratedBy ECO_0000203 NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- befree-2016 importedOn "2016-02-19" NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.