Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_assertion description "[The identification of recurrent cytogenetic abnormalities is hampered by difficulty in culturing tumours and the lack of CD30+ CTCL serial studies comparing genetic changes both at diagnosis and at relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_assertion evidence source_evidence_literature NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_assertion SIO_000772 14595754 NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_assertion wasDerivedFrom befree-20150227 NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_assertion wasGeneratedBy ECO_0000203 NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936780.RAm1FwD70yOALnzrOnt38tYfevSDa7yh4HeXGJdXXBiK8130_provenance.