Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_assertion evidence source_evidence_literature NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_assertion SIO_000772 25447930 NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_assertion wasDerivedFrom befree-2016 NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_assertion wasGeneratedBy ECO_0000203 NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242293.RANi5qIIdJSyO68lSs_p_3s3h73xRr6TDuuhagdBe-WgQ130_provenance.