Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_assertion description "[Furthermore, we examined genetic variations in glucose-6-phosphate dehydrogenase (G6PD) and HBA (?-globin) genes to determine their association with intracranial vasculopathy in children with SCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_assertion evidence source_evidence_literature NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_assertion SIO_000772 22958163 NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_assertion wasDerivedFrom befree-2016 NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_assertion wasGeneratedBy ECO_0000203 NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1011156.RAiScxgRkZB5wEVGLEuy1tPwmdRybrWLXWDV9dn7D11_s130_provenance.