Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion> ?p ?o ?g. }
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- NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion type Assertion NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_head.
- NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion description "[Lamins A/C are encoded by LMNA, a single heterozygous mutation of which causes Hutchinson-Gilford progeria syndrome (HGPS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_provenance.
- NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion evidence source_evidence_literature NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_provenance.
- NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion SIO_000772 26443848 NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_provenance.
- NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion wasDerivedFrom befree-2016 NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_provenance.
- NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_assertion wasGeneratedBy ECO_0000203 NP1294747.RAbRP7kfEentm1Om2bBpTjAiYREKFNIQpVuN41L4BVjbo130_provenance.