Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion> ?p ?o ?g. }
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- NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion type Assertion NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_head.
- NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion description "[Homozygous loss-of-function mutations in TREM2, encoding the triggering receptor expressed on myeloid cells 2 protein, have previously been associated with an autosomal recessive form of early-onset dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_provenance.
- NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion evidence source_evidence_literature NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_provenance.
- NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion SIO_000772 23150934 NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_provenance.
- NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion wasDerivedFrom befree-2016 NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_provenance.
- NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_assertion wasGeneratedBy ECO_0000203 NP1028363.RAlxn4vPI5Q3PbV_qk4a7BReQ9R5xp8sjyr-XeNyHe_us130_provenance.