Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_assertion description "[Early-onset epileptic encephalopathy in a girl carrying a truncating mutation of the ARX gene: rethinking the ARX phenotype in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_assertion evidence source_evidence_literature NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_assertion SIO_000772 23039062 NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_assertion wasDerivedFrom befree-2016 NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_assertion wasGeneratedBy ECO_0000203 NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1018329.RAdRkHfiVELN3my2Ys8cqVzDAaN-KOb6fHkwDnezs5F_c130_provenance.