Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_assertion> ?p ?o ?g. }
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- NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_assertion type Assertion NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_head.
- NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_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." NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_assertion evidence source_evidence_literature NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_assertion SIO_000772 23150934 NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_assertion wasDerivedFrom befree-20150227 NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_assertion wasGeneratedBy ECO_0000203 NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.