Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- befree-2016 importedOn "2016-02-19" NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_assertion wasGeneratedBy ECO_0000203 NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_assertion wasDerivedFrom befree-2016 NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_assertion SIO_000772 22683086 NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_assertion evidence source_evidence_literature NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
- NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.