Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_assertion evidence source_evidence_literature NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_assertion SIO_000772 21264219 NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_assertion wasDerivedFrom befree-20150227 NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_assertion wasGeneratedBy ECO_0000203 NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945505.RAm7cUuCJZYI19lX5PuXTZ_-IvewORYqBodVAhHpgM_eQ130_provenance.