Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_assertion description "[In one of three myxoid nodules and in the surrounding lipoma-like tumor tissue, the translocation t(12;16)(q13;p11), known to be specific for myxoid liposarcoma, was found as the sole chromosomal abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_assertion evidence source_evidence_literature NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_assertion SIO_000772 2193480 NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_assertion wasDerivedFrom befree-20140225 NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_assertion wasGeneratedBy ECO_0000203 NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP248803.RAXVxkpO3xJcVvcQGn4AJZPwA02vl9l_ePlqb98MSsd4E130_provenance.