Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_assertion wasGeneratedBy ECO_0000203 NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_assertion wasDerivedFrom befree-20150227 NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_assertion SIO_000772 23643445 NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_assertion evidence source_evidence_literature NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.
- NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_assertion description "[MRI findings are distinct between patients with POLR3A and 3B mutations, and can provide important clues for the diagnosis, as these patients sometimes have no clinical symptoms suggesting 4H syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860312.RASc2KFGr7SwEbRqLshZvq4Q3mwVAX8lSrsSV_zkDmADM130_provenance.