Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_assertion description "[Furthermore, there is strong evidence against linkage to two Hirschsprung disease (a condition that can cosegregate with neuroblastoma) susceptibility genes, RET and EDNRB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_assertion evidence source_evidence_literature NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_assertion SIO_000772 8758905 NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_assertion wasDerivedFrom befree-2016 NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_assertion wasGeneratedBy ECO_0000203 NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1355601.RAgpVEDpGUf_x0ugIP6L3cq_YHarDf1GdqMlYwzVpn5UE130_provenance.