Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion> ?p ?o ?g. }
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- NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion type Assertion NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_head.
- NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion wasGeneratedBy ECO_0000203 NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_provenance.
- NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion wasDerivedFrom befree-2016 NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_provenance.
- NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion SIO_000772 21212100 NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_provenance.
- NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion evidence source_evidence_literature NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_provenance.
- NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder with no efficient treatment that is caused in the majority of cases by mutations in the gene methyl-CpG binding-protein 2 (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863583.RAPOtkWc_Uq_HKowsfRS8KQb0gVut0rQAoWnWuZkarUIM130_provenance.