Matches in Nanopublications for { ?s ?p "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701012.RAaDa-hU7D7L2Y1ZYzRqHIGr2FoHKIe1_6-iMQwQy2gHk130_provenance.
- NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595488.RAQ6kNZEnYPmtojNjtM_6zHfkRlyz-CIrbLknEAo8_wXM130_provenance.
- assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP965213.RAlKbd5oJc9o4VRkdQYsnw_Tqi4hD0NpoA5-eD3a8IMQE130_assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP965213.RAlKbd5oJc9o4VRkdQYsnw_Tqi4hD0NpoA5-eD3a8IMQE130_provenance.
- NP569910.RAt33kHjQRgzTOXf7TUC0-c4BV5MyyQeHKlHwmazbluF0130_assertion description "[Messenger RNA from NIPA1, NIPA2, CYFIP1, and GCP5 was reduced but detectable in the subjects with Prader-Willi syndrome with the TI deletion, supporting biallelic expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569910.RAt33kHjQRgzTOXf7TUC0-c4BV5MyyQeHKlHwmazbluF0130_provenance.