Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_assertion wasGeneratedBy ECO_0000203 NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_assertion wasDerivedFrom befree-20150227 NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_assertion SIO_000772 7682102 NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_assertion evidence source_evidence_literature NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.
- NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_assertion description "[The regions of allelic deletion on chromosome 11 (11pter-p13), 17 (17pter-p11.2), and 13 (13q) encompass known tumour suppressor loci (WTI, TP53, RBI) which must therefore be candidates for genes contributing to MTC and Pheo development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751053.RAJLwSBtMIqb-_JP38ha0-e8UP8A38a-jUHXmO5fspOHI130_provenance.