Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion type Assertion NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_head.
- NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion description "[Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_provenance.
- NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion evidence source_evidence_literature NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_provenance.
- NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion SIO_000772 15592469 NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_provenance.
- NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion wasDerivedFrom befree-2016 NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_provenance.
- NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_assertion wasGeneratedBy ECO_0000203 NP472329.RAds1vXtJjuVuH3nNeGhw2k5TlhGZl8ytgHvqeRBj8drI130_provenance.