Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_assertion description "[A locus for AR WMS has recently been mapped to chromosome 19p13.3-p13.2 while mutation within the fibrillin-1 gene (15q21.1) was found in one AD WMS family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_assertion evidence source_evidence_literature NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_assertion SIO_000772 14598350 NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_assertion wasDerivedFrom befree-2016 NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_assertion wasGeneratedBy ECO_0000203 NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.
- befree-2016 importedOn "2016-02-19" NP419193.RAesM88BB1nugJGdKUxOBNsCKVpSs_wAdSl7xkwMe5uqM130_provenance.