Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_assertion description "[Mutations in the human ARX gene show unusually heterogeneous clinical presentations, including syndromic and nonsyndromic mental retardation, myoclonic epilepsy with spasticity, and lissencephaly with abnormal genitalia, that are believed to arise from an impairment of the embryonic mechanisms building the anterior central nervous system structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_assertion evidence source_evidence_literature NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_assertion SIO_000772 15376319 NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_assertion wasDerivedFrom befree-20140225 NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_assertion wasGeneratedBy ECO_0000203 NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP770790.RAGlAcToz6uJ3yimAZq5H8sBSBzGcjjkIKkr2WHEcAuBQ130_provenance.