Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_assertion description "[We carried out molecular screening for mutations in the cystic fibrosis transmembrane regulator (CFTR) gene in eight children of Sardinian descent seen because of hypotonic dehydration associated with hyponatremia, hypochloremia, hypokalemia, and metabolic alkalosis; none had pulmonary or pancreatic involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_assertion evidence source_evidence_literature NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_assertion SIO_000772 7543567 NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_assertion wasDerivedFrom befree-2016 NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_assertion wasGeneratedBy ECO_0000203 NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311786.RAJxEq7xkgx4FaOKHLTPKtWSS4_DTFSVv67FWNAeZwY4Y130_provenance.