Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_assertion description "[These data strongly implicate MYLK genetic variants to confer increased risk of sepsis and sepsis-associated ALI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_assertion evidence source_evidence_literature NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_assertion SIO_000772 16399953 NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_assertion wasDerivedFrom befree-20150227 NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_assertion wasGeneratedBy ECO_0000203 NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583939.RAiFUfhgVGpXalKy46jSU5NoWOKWabaYj3kSLwS_XFF28130_provenance.