Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_assertion description "[Mutations in the DELTA-LIKE 3 (DLL3) gene cause the congenital abnormal vertebral segmentation syndrome, spondylocostal dysostosis (SCD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_assertion evidence source_evidence_literature NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_assertion SIO_000772 21147753 NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_assertion wasDerivedFrom befree-20140225 NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_assertion wasGeneratedBy ECO_0000203 NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP702032.RAjM3VW6aAZ1G9yKHjvw7NA3GZBWVGC63AoBl3VfXWsw8130_provenance.