Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion description "[Mutations in CDH3 gene, encoding P-cadherin, are responsible for hypotrichosis with juvenile macular dystrophy (HJMD), which is a rare autosomal recessive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion evidence source_evidence_literature NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion SIO_000772 20140736 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion wasDerivedFrom befree-20140225 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion wasGeneratedBy ECO_0000203 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.