Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_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." NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_assertion evidence source_evidence_literature NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_assertion SIO_000772 21039223 NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_assertion wasDerivedFrom befree-2016 NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_assertion wasGeneratedBy ECO_0000203 NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.
- befree-2016 importedOn "2016-02-19" NP849477.RAQWShiiXMHRIxDnls9RmAwPWTzLjTw0h5n4nobtADsos130_provenance.