Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_assertion description "[In addition, there was strong evidence against linkage to two Hirschsprung disease susceptibility genes (RET and EDNRB), a condition that can cosegregate with neuroblastoma as in one of the kindreds tested here.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_assertion evidence source_evidence_literature NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_assertion SIO_000772 9516825 NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_assertion wasDerivedFrom befree-20140225 NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_assertion wasGeneratedBy ECO_0000203 NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP163821.RAD5c_Yuab2P0xhtQ385TKCJ5IGRS18YwWrMlHElueVZI130_provenance.