Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_assertion description "[We conclude that the inactivating mutations and/or allelic loss of the HRPT2 gene may not play a major role in parathyroid carcinogenesis in secondary HPT due to CKD, but in these cases cancer development may be associated with a heterogeneous genetic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_assertion evidence source_evidence_literature NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_assertion SIO_000772 18338208 NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_assertion wasDerivedFrom befree-2016 NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_assertion wasGeneratedBy ECO_0000203 NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.
- befree-2016 importedOn "2016-02-19" NP660404.RAn7Hi9FSU6aNs37haOYAlN5awK30HJxud7NL0eEPNAJI130_provenance.