Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion> ?p ?o ?g. }
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- NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion type Assertion NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_head.
- NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion description "[The 14q13 region was previously identified by a linkage study of an inherited neurodegenerative condition, idiopathic basal ganglia calcification (IBGC or Fahr syndrome, OMIM:213600/606656), which is often co-morbid with psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_provenance.
- NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion evidence source_evidence_literature NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_provenance.
- NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion SIO_000772 15924306 NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_provenance.
- NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion wasDerivedFrom befree-20150227 NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_provenance.
- NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_assertion wasGeneratedBy ECO_0000203 NP877312.RAaZMre69Z_lPq3gcrUDt5Ud2GNmP1dKbYkEo2DozOBOY130_provenance.