Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_assertion description "[The association of 8 MIF gene polymorphisms (single-nucleotide polymorphisms (SNPs)) (within a 9.7-kb interval on chromosome 22q11.23) with the development of sepsis and ALI in European-descent and African-descent populations was studied next.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_assertion evidence source_evidence_literature NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_assertion SIO_000772 17585860 NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_assertion wasDerivedFrom befree-2016 NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_assertion wasGeneratedBy ECO_0000203 NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.
- befree-2016 importedOn "2016-02-19" NP616414.RAfOpYZqEPQrD4DAe0SxB9pVMQrPoCfc3v7Rygsa-8u3g130_provenance.