Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_assertion description "[The genetic defect was related to leptin and TNFR-II levels in DM1 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_assertion evidence source_evidence_literature NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_assertion SIO_000772 12355336 NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_assertion wasDerivedFrom befree-2016 NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_assertion wasGeneratedBy ECO_0000203 NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.
- befree-2016 importedOn "2016-02-19" NP369314.RA6Md7eVWFfFRKiGijU03ax3I8n4NToWjeL8u0qK6EHC0130_provenance.