Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_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." NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_assertion evidence source_evidence_literature NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_assertion SIO_000772 18338208 NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_assertion wasDerivedFrom befree-20140225 NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_assertion wasGeneratedBy ECO_0000203 NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP335998.RAyEr4WwncnbyVBQx2svX2QjfC2M1nZ_zZVsCjAyN48rk130_provenance.