Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion description "[Three different inheritance patterns have been described, i.e., the X-linked recessive form associated with arginine vasopressin V2 receptor (AVPR2) gene mutations, the autosomal recessive and dominant forms of CNDI associated with mutations in the aquaporin-2 (AQP2) gene encoding the vasopressin-regulated water channel of the renal collecting duct.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion evidence source_evidence_literature NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion SIO_000772 19461158 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion wasDerivedFrom befree-20150227 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion wasGeneratedBy ECO_0000203 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.