Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_assertion description "[Recent studies of the variation within families harboring PKD1 mutations indicate that genetic background may account for 32 to 42% of the variance in estimated GFR (eGFR) before ESRD and 43 to 78% of the variance in age at ESRD onset, but the genetic modifiers are unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_assertion evidence source_evidence_literature NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_assertion SIO_000772 20616171 NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_assertion wasDerivedFrom befree-20140225 NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_assertion wasGeneratedBy ECO_0000203 NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP414980.RA6NtVPcM2agkpbjzs49h-e_TIe_0cqOCcufLd-WGJaHE130_provenance.