Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_assertion description "[Wagner syndrome (WGN1) is associated with mutations in versican (CSPG2) and snowflake vitreoretinal degeneration (SVD) with a mutation in a potassium channel (KCNJ13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_assertion evidence source_evidence_literature NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_assertion SIO_000772 18309337 NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_assertion wasDerivedFrom befree-20150227 NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_assertion wasGeneratedBy ECO_0000203 NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP332971.RAwQMkP0bywXsL08tiKTq6wgiloL4zQCdA1ojGCR5NRs4130_provenance.