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- source_evidence_literature type ECO_0000212 NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_assertion description "[the aims of this study were to identify HJV and HAMP mutations and to analyze their impact on HH phenotype in non-p.C282Y homozygous individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_assertion evidence source_evidence_literature NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_assertion SIO_000772 21039223 NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_assertion wasDerivedFrom befree-2016 NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_assertion wasGeneratedBy ECO_0000203 NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.
- befree-2016 importedOn "2016-02-19" NP849474.RAtM_8bBQv4UC4XJfaQLoZQsLMbL_Z49FbAqgyNGjH2f8130_provenance.