Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_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." NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_assertion evidence source_evidence_literature NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_assertion SIO_000772 22683086 NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_assertion wasDerivedFrom befree-20140225 NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_assertion wasGeneratedBy ECO_0000203 NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.