Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_assertion wasGeneratedBy ECO_0000203 NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_assertion wasDerivedFrom befree-20140225 NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_assertion SIO_000772 2539641 NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_assertion evidence source_evidence_literature NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_assertion description "[These loci are near the translocation breakpoint seen in the t(X;18) (p11.2;q11.2), which is characteristic of synovial sarcoma, and the chromosome 14q32 breakpoints seen in ataxia telangiectasia and other T cell malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP737007.RAJ0wySKrJcW_qwMpVUzZ5_NLITZhV0ZqssMwbEyea6TA130_provenance.