Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_assertion wasGeneratedBy ECO_0000203 NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_assertion wasDerivedFrom befree-20150227 NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_assertion SIO_000772 12428212 NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_assertion evidence source_evidence_literature NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.
- NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_assertion description "[Physical mapping of the breakpoints of a pericentric inversion of the X chromosome (46,X,inv[X][p21q27]) in a female patient with mild mental retardation revealed localization of the Xp breakpoint in the IL1RAPL gene at Xp21.3 and the Xq breakpoint near the SOX3 gene (SRY [sex determining region Y]-box 3) (GenBank accession number NM_005634) at Xq26.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860532.RAUJMBexA5i9W9wxGER-z7QnELMTgExSSKLz2jY3dTF_s130_provenance.