Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_assertion description "[These novel mutations have also resulted in osteopenia, bilateral sensorineural deafness and pancreatic exocrine insufficiency, features that have not previously been associated with GLIS3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_assertion evidence source_evidence_literature NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_assertion SIO_000772 21139041 NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_assertion wasDerivedFrom befree-20150227 NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_assertion wasGeneratedBy ECO_0000203 NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978049.RAQ9fff3pFFXksAYPHYZLU0SiVyBJNzv01CAFX3_qQTwc130_provenance.