Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_assertion description "[Physical mapping of the breakpoints localized the chromosome 6 breakpoint within an intron of the gene lipoma HMGIC fusion partner-like 5 (LHFPL5) whereas the chromosome 17 breakpoint was mapped to the first intron of the 182-FIP gene encoding the Fragile X Mental Retardation Protein Interacting Protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_assertion evidence source_evidence_literature NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_assertion SIO_000772 16395596 NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_assertion wasDerivedFrom befree-20140225 NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_assertion wasGeneratedBy ECO_0000203 NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269613.RAGsjG1Bq8mRtU42eLnl1wg-euwOG3Kb7al9mwLhTslyA130_provenance.