Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion type Assertion NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_head.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion wasGeneratedBy ECO_0000203 NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_provenance.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion wasDerivedFrom lhgdn-20090331 NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_provenance.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion SIO_000772 17457594 NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_provenance.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion evidence source_evidence_literature NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_provenance.
- NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_assertion description "[Frontotemporal dementia with inclusion body myopathy and Paget's disease of bone (IBMPFD) 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." NP134990.RAdMvE_HiLlvdAYeR9UwGkIi47s1rVCLszimI5OHywd-k130_provenance.