Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_assertion description "[Mouse models of XLAG, ISSX and other human ARX mutations demonstrate a direct genotype-phenotype correlation in ARX-related neurologic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_assertion evidence source_evidence_literature NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_assertion SIO_000772 24236044 NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_assertion wasDerivedFrom befree-20150227 NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_assertion wasGeneratedBy ECO_0000203 NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978116.RAb8NRhGWOA8ppi5ERKSFNLJWIsVj53Q6ZXTi0bFIM0p0130_provenance.