Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_assertion description "[In conclusion, chromosomal abnormalities are frequent in ATCs associated with FTC, but uncommon in those associated with PTC and in ATCs with no associated differentiated thyroid cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_assertion evidence source_evidence_literature NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_assertion SIO_000772 12729478 NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_assertion wasDerivedFrom befree-20150227 NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_assertion wasGeneratedBy ECO_0000203 NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788615.RAeRnGjKNJnFYrIN87RZECnyaRrN8_lzBsFEUdsPmi5pM130_provenance.