Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_assertion wasGeneratedBy ECO_0000203 NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_assertion wasDerivedFrom befree-2016 NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_assertion SIO_000772 24402736 NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_assertion evidence source_evidence_literature NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.
- NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_assertion description "[Furthermore, germline testing for HRPT2 mutation in patients presenting with parathyroid carcinoma often identifies occult HPT-JT syndrome even in the absence of a family history or other syndromic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143161.RAk4s59yyA0wtY9Z-AmizcU2uPc8CkZ36QAKdOgZx5vOM130_provenance.