Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_assertion wasGeneratedBy ECO_0000203 NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_assertion wasDerivedFrom befree-20150227 NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_assertion SIO_000772 1868037 NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_assertion evidence source_evidence_literature NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.
- NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_assertion description "[Chromosome 10 exhibited a complex deletion pattern with terminal deletions of the p or the q arm (2 cases each), a deletion pattern that could be interpreted as nonreciprocal translocations of the q arm (2 cases), or allelic losses on all informative loci, suggesting monosomy (2 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902548.RA5SoqSgwHm_hyg_9X9_h-BJlFT-gg30_LlHXd-fsQfmE130_provenance.