Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_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." NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_assertion evidence source_evidence_literature NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_assertion SIO_000772 18338208 NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_assertion wasDerivedFrom befree-20150227 NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_assertion wasGeneratedBy ECO_0000203 NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP943623.RAh1fBv1-4ncEPItnoYZrARegpiFs3EINfpB1u1zyBDC0130_provenance.