Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_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." NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_assertion evidence source_evidence_literature NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_assertion SIO_000772 21288648 NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_assertion wasDerivedFrom befree-2016 NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_assertion wasGeneratedBy ECO_0000203 NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.
- befree-2016 importedOn "2016-02-19" NP869695.RAzS7roj7BGUHpzdYhMqBmjJP_yypLejWmIzwn20ZhIeM130_provenance.