Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_assertion description "[Of 6 cases, 1 (16%) showed no evidence of TSPY1; in this case, which occurred in a gravida 2 para 2 woman, 2 X chromosomes were present in the nonneoplastic ovary, the gonadoblastoma, and associated dysgerminoma and granulosa cell tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_assertion evidence source_evidence_literature NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_assertion SIO_000772 20656323 NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_assertion wasDerivedFrom befree-2016 NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_assertion wasGeneratedBy ECO_0000203 NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.
- befree-2016 importedOn "2016-02-19" NP828009.RAQ3HVbew1XeNKOwpDl8jseUIele3rJs7aX0ZGqQbGeO4130_provenance.