Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_assertion description "[L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_assertion evidence source_evidence_literature NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_assertion SIO_000772 7920660 NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_assertion wasDerivedFrom befree-20140225 NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_assertion wasGeneratedBy ECO_0000203 NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP172925.RAfOyCvwGstEkiGQNkNKkXf5DmEz_2HPeBVIDW36Z-hHM130_provenance.