Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_assertion wasGeneratedBy ECO_0000203 NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_assertion wasDerivedFrom befree-20140225 NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_assertion SIO_000772 23434763 NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_assertion evidence source_evidence_literature NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_assertion description "[To identify the cause of OI in eight children with severe bone fragility and a clinical diagnosis of OI type IV who had had negative results on COL1A1/COL1A2 Sanger sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690281.RAcV1MBV_zA8NwN382LFrIyt0cQmKErhaWJTcnb7vpOqQ130_provenance.