Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_assertion description "[Monoallelic expression of NLGN4 was seen in this subject and in 11 of 14 informative autistic and non-autistic females using a single nucleotide polymorphism found at 3' UTR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_assertion evidence source_evidence_literature NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_assertion SIO_000772 16648374 NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_assertion wasDerivedFrom befree-20140225 NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_assertion wasGeneratedBy ECO_0000203 NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP501710.RAG6_eeO41ywm4HX-Voplpbz1HHxi_cMdkUKEcempvOEc130_provenance.