Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_assertion evidence source_evidence_literature NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_assertion SIO_000772 18193163 NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_assertion wasDerivedFrom befree-2016 NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_assertion wasGeneratedBy ECO_0000203 NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.
- befree-2016 importedOn "2016-02-19" NP649784.RAAuq2YkaZ9JLxXevWa9id5_V6cA-xgyBAa9j1NIayiSk130_provenance.