Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion type Assertion NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_head.
- NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion wasGeneratedBy ECO_0000203 NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_provenance.
- NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion wasDerivedFrom befree-2016 NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_provenance.
- NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion SIO_000772 23335487 NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_provenance.
- NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion evidence source_evidence_literature NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_provenance.
- NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_assertion description "[Our data reveal a broad range of epimutations exist in certain imprinting syndromes, with the exception of Prader-Willi syndrome and Angelman syndrome patients that are associated with solitary SNRPN-DMR defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045448.RAe_W6Hj8eYURajcN0KxKDBqMDt93BGzopn-rJFFLuPqs130_provenance.