Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_assertion description "[SSCP analyses followed by direct DNA sequencing showed GCG-->GTG (Ala-->Val) transition mutation in codon 253 of the cytoplasmic carboxyl terminal of the Cx43 gene in 1 of 31 (3%) benign meningiomas and 1 of 14 (7%) anaplastic meningiomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_assertion evidence source_evidence_literature NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_assertion SIO_000772 9210880 NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_assertion wasDerivedFrom befree-20150227 NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_assertion wasGeneratedBy ECO_0000203 NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420379.RAn7lAnhItYe3uKoUC4Kal5A3SGicmU0o2rSVkzRZw1sA130_provenance.