Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_assertion description "[(1) NKX2.5 mutation c.512insGC is associated with ASDs, syncope and sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_assertion evidence source_evidence_literature NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_assertion SIO_000772 20932824 NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_assertion wasDerivedFrom befree-2016 NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_assertion wasGeneratedBy ECO_0000203 NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP844558.RAwY4p4v-mvnSbZja19KMmcexKeNxblGyhLdPt-y-vH0Q130_provenance.