Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_assertion description "[To report the clinical phenotype in patients with a retinal dystrophy associated with novel mutations in the MER tyrosine kinase (MERTK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_assertion evidence source_evidence_literature NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_assertion SIO_000772 20300561 NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_assertion wasDerivedFrom befree-2016 NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_assertion wasGeneratedBy ECO_0000203 NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.
- befree-2016 importedOn "2016-02-19" NP800977.RAZ2mDsbJ2a9wTMuPQGNC4b3a_wH6CLgrAl2RJ86QFl2g130_provenance.