Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion> ?p ?o ?g. }
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- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion type Assertion NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_head.
- 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.