Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP787657.RAPBytGEg1IkVFSVKmqELakToCKIMh5w8I8peQEIWlICc130_provenance.