Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP422613.RAbBFvJ7m7uNPRA-Uv3-E6Y29J5LZ9dfUZwuSDzJ8Sg2Q130_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." NP422613.RAbBFvJ7m7uNPRA-Uv3-E6Y29J5LZ9dfUZwuSDzJ8Sg2Q130_provenance.
- 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." provenance.
- NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_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." NP294454.RA_-WWBEqJcETx8M1Q5aT3KS45j1LikBihG6KHMZ_aux4130_provenance.
- NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_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." NP294455.RA581yOH-agBmuwQa7eq3RsOdB4cGAkiPrbI_XPijs6ik130_provenance.
- NP294456.RAbMXMpXDGUPngbmJnTRReHgIWaqWREem8209L5BabE0Y130_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." NP294456.RAbMXMpXDGUPngbmJnTRReHgIWaqWREem8209L5BabE0Y130_provenance.
- NP422338.RAKFA43opxctWdgw8D-biL4lFouI4rS5-QQRhuQU8CLV0130_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." NP422338.RAKFA43opxctWdgw8D-biL4lFouI4rS5-QQRhuQU8CLV0130_provenance.
- 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." provenance.
- NP294453.RAng1scRarKebaLUBg-o5F_ZGpNDunnmzLQjiC20syI4E130_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." NP294453.RAng1scRarKebaLUBg-o5F_ZGpNDunnmzLQjiC20syI4E130_provenance.