Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_assertion description "[TTR gene analysis has useful applications in genetic counselling, including prenatal diagnosis, in identifying the cause of seemingly sporadic cases of amyloid neuropathy, and in epidemiological studies of FAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_assertion evidence source_evidence_literature NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_assertion SIO_000772 2564060 NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_assertion wasDerivedFrom befree-20140225 NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_assertion wasGeneratedBy ECO_0000203 NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP837706.RA1VR_C7inYv_CUF392Jg4tPfcolRRh3lUKWqJMjg2zfs130_provenance.