Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion> ?p ?o ?g. }
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- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion type Assertion NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_head.
- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion wasGeneratedBy ECO_0000203 NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_provenance.
- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion wasDerivedFrom befree-20140225 NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_provenance.
- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion SIO_000772 11749051 NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_provenance.
- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion evidence source_evidence_literature NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_provenance.
- NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_assertion description "[Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844266.RAJzaswJNZ0DwgWbTTDBOtiGzMXx8Ms2zYABF6Yf9SyeI130_provenance.