Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_assertion description "[The human SNRPN gene maps within Chromosome (Chr) 15q11-q13, the region responsible for Prader-Willi syndrome (PWS) and Angelman syndrome (AS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_assertion evidence source_evidence_literature NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_assertion SIO_000772 9745031 NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_assertion wasDerivedFrom befree-2016 NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_assertion wasGeneratedBy ECO_0000203 NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404315.RANvWWX87uE9IsNK8peQlkQVvx7q9kcsrUnXmSjDvORjo130_provenance.