Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_assertion description "[If future carefully controlled studies confirm the hypothesis of influence of hypermelanotic or hypomelanotic skin status of the individual patients on severity in phenotypic expression of homozygous SCD, genetic and pharmacological interventions aimed at regulation of melanin production may play a role in alleviating the severity in phenotypic expression of SCD in affected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_assertion evidence source_evidence_literature NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_assertion SIO_000772 21288648 NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_assertion wasDerivedFrom befree-20150227 NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_assertion wasGeneratedBy ECO_0000203 NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP701874.RAb14uufc6ZUFdFWFtetoZPsDPctXHakcpA06-mbw-vDU130_provenance.