Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion> ?p ?o ?g. }
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- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion type Assertion NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_head.
- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_provenance.
- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion evidence source_evidence_literature NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_provenance.
- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion SIO_000772 22532172 NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_provenance.
- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion wasDerivedFrom befree-2016 NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_provenance.
- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion wasGeneratedBy ECO_0000203 NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_provenance.