Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_assertion description "[The common aberration found in these two t-MDS cases was the fragility of chromosome 5 and monosomy of chromosome 18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_assertion evidence source_evidence_literature NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_assertion SIO_000772 12505257 NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_assertion wasDerivedFrom befree-2016 NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_assertion wasGeneratedBy ECO_0000203 NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.
- befree-2016 importedOn "2016-02-19" NP378940.RANknPYYbNrSp03bthJ08ZMYHnlRnvNfWOGtHW2jR3LnI130_provenance.