Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion description "[Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion evidence source_evidence_literature NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion SIO_000772 17959774 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion wasDerivedFrom befree-20150227 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_assertion wasGeneratedBy ECO_0000203 NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936061.RAD810zqszdxf7aGRQPdvPk90tHv6gn3tkxdP53hk8_0s130_provenance.