Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- befree-2016 importedOn "2016-02-19" NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_assertion wasGeneratedBy ECO_0000203 NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_assertion wasDerivedFrom befree-2016 NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_assertion SIO_000772 18371931 NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_assertion evidence source_evidence_literature NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.
- NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_assertion description "[In humans, we show that NPHP3 mutations can cause a broad clinical spectrum of early embryonic patterning defects comprising situs inversus, polydactyly, central nervous system malformations, structural heart defects, preauricular fistulas, and a wide range of congenital anomalies of the kidney and urinary tract (CAKUT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662673.RANfIGoaBgmafE0OX99Gacz4v7qWKzdKoVncjvru4kb4E130_provenance.