Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_assertion description "[Here we describe the construction and characterization of DNA libraries for the Langer-Giedion syndrome chromosome region (LGCR, 8q23-24.1), Wilms tumor chromosome region 1 (WT1, 11p13), Prader-Willi syndrome/Angelman syndrome chromosome region (PWCR/ANCR, 15q11.2-12), meningioma chromosome region (MGCR, 22q12-13), and fragile X chromosome region (FRAXA, Xq27.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_assertion evidence source_evidence_literature NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_assertion SIO_000772 2159949 NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_assertion wasDerivedFrom befree-20150227 NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_assertion wasGeneratedBy ECO_0000203 NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP765015.RAvHFbN8SfRDgqvmw-3L3CQ2evm4ml27_7ODdd2dEe26w130_provenance.