Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_assertion evidence source_evidence_literature NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_assertion SIO_000772 21739600 NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_assertion wasDerivedFrom befree-2016 NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_assertion wasGeneratedBy ECO_0000203 NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.
- befree-2016 importedOn "2016-02-19" NP908153.RA4T5aZrEpMEIdMUhCL08ba9bljiUL1FZdoq4hXSCrwQs130_provenance.