Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion wasGeneratedBy ECO_0000203 NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion wasDerivedFrom befree-20140225 NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion SIO_000772 10978357 NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion evidence source_evidence_literature NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_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." NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.