Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion type Assertion NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_head.
- NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion description "[Recently, it has been shown that genetic defects of human DAP12/KARAP and TREM-2 result in a rare syndrome characterized by bone cysts and presenile dementia called Nasu-Hakola disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_provenance.
- NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion evidence source_evidence_literature NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_provenance.
- NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion SIO_000772 12913093 NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_provenance.
- NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion wasDerivedFrom befree-20150227 NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_provenance.
- NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_assertion wasGeneratedBy ECO_0000203 NP764258.RA7iNRO-P2MHyZXPLY9RUTfL0oowtWlB8VNKeVJUHyY5s130_provenance.