Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_assertion description "[Of the 51 patients in whom the molecular extent of the chromosomal deletion could be delineated by pulsed-field gel electrophoresis (PFGE) and/or fluorescent in situ hybridization (FISH), 39 (approximately 76%) had the common SMS deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_assertion evidence source_evidence_literature NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_assertion SIO_000772 14614393 NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_assertion wasDerivedFrom befree-20140225 NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_assertion wasGeneratedBy ECO_0000203 NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806438.RAf8fI9_UNXB29JTag_-M6oHX16uezTUBh_HCkXvjUNOA130_provenance.