Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_assertion description "[We conclude that LADA is a familial disease involving most likely gene defects leading to a slow progressive beta-cell destruction and insulin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_assertion evidence source_evidence_literature NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_assertion SIO_000772 10663218 NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_assertion wasDerivedFrom befree-20150227 NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_assertion wasGeneratedBy ECO_0000203 NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1007870.RAz2fBNkM9PNss_Py-MI71jcSItySGmPYpVCixvbUB6Pc130_provenance.