Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_assertion description "[The findings expand the mutational spectrum of NKX2-5 linked to DCM and provide novel insight into the molecular mechanisms underlying DCM, contributing to the antenatal prophylaxis and allele-specific management of DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_assertion evidence source_evidence_literature NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_assertion SIO_000772 25503402 NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_assertion wasDerivedFrom befree-2016 NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_assertion wasGeneratedBy ECO_0000203 NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247897.RApl0IH3z2ERJd6p4K-lvmkokOXtEUSDV8NX4ABcscdXk130_provenance.