Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_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." NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_assertion evidence source_evidence_literature NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_assertion SIO_000772 21288648 NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_assertion wasDerivedFrom befree-2016 NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_assertion wasGeneratedBy ECO_0000203 NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.
- befree-2016 importedOn "2016-02-19" NP869696.RA2c0cwQ0Xcay9JqdCd7G2O28OtK18YxQcD2mrxsxezM0130_provenance.