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- source_evidence_literature type ECO_0000212 NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_assertion description "[Within nine dentin dysplasia (DD) (type II) and dentinogenesis imperfecta (type II and III) patient/families, seven have 1 of 4 net -1 deletions within the approximately 2-kb coding repeat domain of the DSPP gene while the remaining two patients have splice-site mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_assertion evidence source_evidence_literature NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_assertion SIO_000772 18521831 NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_assertion wasDerivedFrom befree-20150227 NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_assertion wasGeneratedBy ECO_0000203 NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP840120.RAAhidZoSEGBFlAzn0GIrdT0QSNfoZJ5_bFuGjeymR8RI130_provenance.