Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_assertion description "[These results do not define a clear cataract-SORD deficiency etiopathogenic relationship, nevertheless, they strongly suggest activity polymorphism in human red cell SORD, which would be highly relevant not only to the study of cataracts but of other major complications in diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_assertion evidence source_evidence_literature NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_assertion SIO_000772 7152518 NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_assertion wasDerivedFrom befree-20140225 NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_assertion wasGeneratedBy ECO_0000203 NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.
- befree-20140225 importedOn "2014-02-25" NP801595.RA_GqMf_cZqLPV2XtHvW4NVgO24hKyX1wdapGuVFxEuro130_provenance.