Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_assertion description "[Brain magnetic resonance imaging (MRI) of all patients showed no brain malformations in contrast to the patients with a premature termination mutation in other exons of ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_assertion evidence source_evidence_literature NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_assertion SIO_000772 20384723 NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_assertion wasDerivedFrom befree-2016 NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_assertion wasGeneratedBy ECO_0000203 NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.
- befree-2016 importedOn "2016-02-19" NP805576.RA0hG8Tw_KCXensVqGp1P1NtzCN0V6ZuZ7BZem19oYNRk130_provenance.