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- source_evidence_literature type ECO_0000212 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_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." NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion evidence source_evidence_literature NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion SIO_000772 10982188 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion wasDerivedFrom befree-20150227 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_assertion wasGeneratedBy ECO_0000203 NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779024.RAn54D4aoYQWh4asfesr0Ros-oiDiluko_VD-udi9PArE130_provenance.