Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_assertion description "[Four of nine informative fetal rhabdomyomas and embryonal rhabdomyosarcomas showed loss of heterozygosity (LOH) in the PTCH region with two of these (one fetal rhabdomyoma and one embryonal rhabdomyosarcoma) also showing LOH in the SUFU region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_assertion evidence source_evidence_literature NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_assertion SIO_000772 16294371 NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_assertion wasDerivedFrom befree-20140225 NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_assertion wasGeneratedBy ECO_0000203 NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP836991.RAJ0QCPSjmsJ3dlOxCpwNY0d4LVAYj6Mj3sI04VJVbWsU130_provenance.