Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- befree-2016 importedOn "2016-02-19" NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_assertion wasGeneratedBy ECO_0000203 NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_assertion wasDerivedFrom befree-2016 NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_assertion SIO_000772 19542869 NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_assertion evidence source_evidence_literature NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.
- NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_assertion description "[Specimens with morphologic features suggestive of CHM yet retaining p57 expression should be subjected to molecular genotyping to establish a definitive diagnosis because misclassification as PHM underestimates the risk of persistent gestational trophoblastic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746485.RAD9EsPn45NCehHYMk8_ZsjvQrxnOb4klgX-CljKOAi8A130_provenance.