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- source_evidence_literature type ECO_0000212 NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_assertion description "[Restudy of the original DFN-1 family showed that the deafness is part of a progressive X linked recessive syndrome, which includes visual disability leading to cortical blindness, dystonia, fractures, and mental deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_assertion evidence source_evidence_literature NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_assertion SIO_000772 7643352 NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_assertion wasDerivedFrom befree-20150227 NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_assertion wasGeneratedBy ECO_0000203 NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP353098.RA4HAPYT8EMOWkkk6uhjWuHHAhymaiXlKR-WdY_RLFjEw130_provenance.