Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP910389.RAehW5tSkBxNkEAW0uB89u5gn9m1bV2NZnGtYK0bgWqy4130_provenance.