Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP589811.RAiZisymcTSKO3L8G2VWx82Sz7qdHWrO59HipwJSSKCOw130_provenance.