Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion evidence source_evidence_curated NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion SIO_000772 23561846 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion wasDerivedFrom uniprot-2016 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion wasGeneratedBy ECO_0000218 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.