Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_assertion evidence source_evidence_literature NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_assertion SIO_000772 10982188 NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_assertion wasDerivedFrom befree-20150227 NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_assertion wasGeneratedBy ECO_0000203 NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779014.RAafGdAGS03E0VprC3FCrQZ90YgbPGZAlkciAdr3-YrSw130_provenance.