Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- befree-2016 importedOn "2016-02-19" NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion wasGeneratedBy ECO_0000203 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion wasDerivedFrom befree-2016 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion SIO_000772 16361827 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion evidence source_evidence_literature NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion description "[There are three inheritance patterns of CNDI: the X-linked recessive form associated with vasopressin V2 receptor gene mutations, and the autosomal recessive and dominant forms associated with aquaporin-2 gene (AQP2) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.