Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_assertion description "[The c.429_452dup24 of the ARX gene is a rare genetic anomaly, leading to X-Linked Intellectual Disability without brain malformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_assertion evidence source_evidence_literature NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_assertion SIO_000772 24528893 NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_assertion wasDerivedFrom befree-20150227 NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_assertion wasGeneratedBy ECO_0000203 NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835519.RAxDg_0XkvM0o20IE0GKQ6ENzkCqktIFIC3I-W6BIDY4Y130_provenance.