Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765338.RAhTiyL8ab8fLXKRcT4ICmyK805J9EU-SgIHeA2VaoCrM130_provenance.
• NP546340.RAJbViGOj0kC0-RSw8E0oVpAWDib43n8WqDOvVPWTj0-Y130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546340.RAJbViGOj0kC0-RSw8E0oVpAWDib43n8WqDOvVPWTj0-Y130_provenance.
• NP365776.RA7ZtxEmKGbf9amrymErOkDMI_O7UQcku8UBAOAsNC72o130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365776.RA7ZtxEmKGbf9amrymErOkDMI_O7UQcku8UBAOAsNC72o130_provenance.
• assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP282769.RA7_-hgUiKkdz-FduImB55SqzggQVt6_TcJHhrIKW9i0A130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282769.RA7_-hgUiKkdz-FduImB55SqzggQVt6_TcJHhrIKW9i0A130_provenance.
• NP365211.RAF-D-LK9aiENeYrS2s1q_Nil_xgX_WfBJgCW1xe3F8cc130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365211.RAF-D-LK9aiENeYrS2s1q_Nil_xgX_WfBJgCW1xe3F8cc130_provenance.
• NP282770.RAXi4VrCh48-wBjtuXIdw0Z9Qr4ltIOHhUNm7zA2ZCfWs130_assertion description "[However, the similarity between the distal colonic aganglionosis in Hirschsprung disease and that due to EDN3 or EDNRB mutations led to the hypothesis that levels of expression of these genes might be affected in the absence of mutation, thus causing the Hirschsprung disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282770.RAXi4VrCh48-wBjtuXIdw0Z9Qr4ltIOHhUNm7zA2ZCfWs130_provenance.