Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_assertion description "[Congenital nephrotic syndrome of the Finnish type (CNF) is a rare autosomal recessively inherited disease characterised by intrauterine onset of massive urinary loss of proteins, 90% of which is albumin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_assertion evidence source_evidence_literature NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_assertion SIO_000772 7742232 NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_assertion wasDerivedFrom befree-20140225 NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_assertion wasGeneratedBy ECO_0000203 NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650556.RAmRzwpjPSq1qngjUqXjtXsv1nE4j6Ed8r3saB9CW9Uww130_provenance.