Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_assertion description "[Collectively, identification of mutations in the MRP6 gene provides the basis to examine the pathomechanisms of PXE and allows development of DNA-based carrier detection, prenatal testing, and preimplantation genetic diagnosis in families with a history of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_assertion evidence source_evidence_literature NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_assertion SIO_000772 10811882 NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_assertion wasDerivedFrom befree-20150227 NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_assertion wasGeneratedBy ECO_0000203 NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP679561.RA_wXrFN3Ttg7gd2jcg_3ZM9lUPmPXK_UioTKrfJGPIlU130_provenance.