Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_assertion wasGeneratedBy ECO_0000203 NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_assertion wasDerivedFrom befree-20150227 NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_assertion SIO_000772 18285834 NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_assertion evidence source_evidence_literature NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.
- NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_assertion description "[Putative loss-of-function mutations in PROKR2 or PROK2, encoding prokineticin receptor-2 (a G protein-coupled receptor), and one of its ligands, prokineticin-2, respectively, have recently been reported in approximately 10% of Kallmann syndrome affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926834.RAzO_KHF7ZNle2t5XW63QU64eUTKEwoIeNEQ23LWH4ELg130_provenance.