Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_assertion wasGeneratedBy ECO_0000218 NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_assertion wasDerivedFrom uniprot-20150221 NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_assertion SIO_000772 17632511 NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_assertion evidence source_evidence_curated NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.
- NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_assertion description "[Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88.RAUDMdBX0VyEG-qo46nyomiRL1kRFTen3TSsJ7EI0rE3g130_provenance.