Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_assertion description "[In addition, these findings are compatible with a modifying role for the centromeric SMN genes and the NAIP genes in the severity of the SMA phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_assertion evidence source_evidence_literature NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_assertion SIO_000772 8957014 NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_assertion wasDerivedFrom befree-2016 NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_assertion wasGeneratedBy ECO_0000203 NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1363988.RAPpM-iiqcCWv25yNC7ZgDErXYSKclFiWUm66AqqX0dL8130_provenance.