Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion> ?p ?o ?g. }
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- NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion type Assertion NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_head.
- NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion description "[Since RS is mostly caused by mutations in the MECP2 gene, transgenic animal models such as the Mecp2-deleted (Mecp2-null) mouse have been employed to study neurological symptoms and brain function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion evidence source_evidence_literature NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion SIO_000772 17237885 NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion wasDerivedFrom befree-2016 NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_assertion wasGeneratedBy ECO_0000203 NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.