Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion evidence source_evidence_literature NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion SIO_000772 11773000 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion wasDerivedFrom befree-20140225 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion wasGeneratedBy ECO_0000203 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.