Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_assertion wasGeneratedBy ECO_0000203 NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_assertion wasDerivedFrom befree-20150227 NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_assertion SIO_000772 11566339 NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_assertion evidence source_evidence_literature NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.
- NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_assertion description "[There were also frequently observed secondary changes such as chromosome 1 rearrangement leading to trisomy of 1q and loss of tp53 from the deleted chromosome 17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751340.RA45mbgS7Xgmbt9DkZvTqZazj8GanBj9ULSDo5m55lqGw130_provenance.