Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion> ?p ?o ?g. }
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- NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion type Assertion NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_head.
- NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion description "[Its human homologue, RAE28, is located on chromosome 12p13, which frequently is associated with chromosomal abnormalities and loss of heterozygosity in patients with hematologic malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion evidence source_evidence_literature NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion SIO_000772 11164110 NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion wasDerivedFrom befree-20140225 NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_assertion wasGeneratedBy ECO_0000203 NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.