Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion> ?p ?o ?g. }
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- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion type Assertion NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_head.
- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_provenance.
- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion evidence source_evidence_literature NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_provenance.
- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion SIO_000772 16317258 NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_provenance.
- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion wasDerivedFrom befree-20140225 NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_provenance.
- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion wasGeneratedBy ECO_0000203 NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_provenance.