Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_assertion description "[Genetic variation in hepatic glucose-6-phosphatase system genes in cases of sudden infant death syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_assertion evidence source_evidence_literature NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_assertion SIO_000772 17354259 NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_assertion wasDerivedFrom befree-2016 NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_assertion wasGeneratedBy ECO_0000203 NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.
- befree-2016 importedOn "2016-02-19" NP598610.RARd-9IK6cvUtl8CHoYcP1YJt_fBBXGcMdPMFdBbBTn4E130_provenance.