Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_assertion description "[Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_assertion evidence source_evidence_literature NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_assertion SIO_000772 21270828 NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_assertion wasDerivedFrom befree-2016 NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_assertion wasGeneratedBy ECO_0000203 NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.
- befree-2016 importedOn "2016-02-19" NP868119.RA5W21U-onh3bT4pPtFCcnAnJqhnGt72_zpJTFMZBEh4I130_provenance.