Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_assertion description "[Here, we describe a unique patient with a small isolated 9p terminal deletion, characterized by array-CGH and FISH, who shows a complex phenotype with multiple physical anomalies, resembling the 9p-syndrome, disorder of sex development with gonadoblastoma, congenital heart defect and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_assertion evidence source_evidence_literature NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_assertion SIO_000772 22821627 NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_assertion wasDerivedFrom befree-20150227 NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_assertion wasGeneratedBy ECO_0000203 NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470221.RAZsSwTsZXnmEaQDDTUj1tnFK7sDrPEThutmVkIX0G1no130_provenance.