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- NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_assertion type Assertion NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_head.
- NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget disease of bone is a rare, autosomal-dominant disorder caused by mutations in the gene valosin-containing protein (VCP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_provenance.
- NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_assertion evidence source_evidence_literature NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_provenance.
- NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_assertion SIO_000772 17279000 NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_provenance.
- NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_assertion wasDerivedFrom befree-20140225 NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_provenance.
- NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_assertion wasGeneratedBy ECO_0000203 NP240060.RAYh5u2wVPiRdMH4XzBTLwPVyopVpGnscrUPfC350mvUU130_provenance.