Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_assertion wasGeneratedBy ECO_0000203 NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_assertion wasDerivedFrom befree-20150227 NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_assertion SIO_000772 15001591 NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_assertion evidence source_evidence_literature NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.
- NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_assertion description "[Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400693.RA9PLHCvN7uScCZkVMkp8kuw3Kgta2mtuhKf-P6xv-ksY130_provenance.