Matches in Nanopublications for { ?s ?p "[In humans, mutations of RET or RET ligands are associated with the congenital abnormality Hirschsprung disease (HSCR) in which nerves and ganglia of the hind gut are absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP670511.RAd1hcMZPBRvEuYGNuiI5C_l4oqm2zWhRwBstB8VnpLkU130_assertion description "[In humans, mutations of RET or RET ligands are associated with the congenital abnormality Hirschsprung disease (HSCR) in which nerves and ganglia of the hind gut are absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670511.RAd1hcMZPBRvEuYGNuiI5C_l4oqm2zWhRwBstB8VnpLkU130_provenance.
- assertion description "[In humans, mutations of RET or RET ligands are associated with the congenital abnormality Hirschsprung disease (HSCR) in which nerves and ganglia of the hind gut are absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_assertion description "[In humans, mutations of RET or RET ligands are associated with the congenital abnormality Hirschsprung disease (HSCR) in which nerves and ganglia of the hind gut are absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321150.RAYfMm2fINqbHDKjK3xCk8ZN_rvI8KRfmr0pVk42xvoSQ130_provenance.