Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion description "[Also studied were two siblings who were homozygous for the PITX3 mutation who had microphthalmia and significant neurologic impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion evidence source_evidence_literature NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion SIO_000772 16565358 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion wasDerivedFrom befree-20150227 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_assertion wasGeneratedBy ECO_0000203 NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP626565.RAqQHq9DHfSAcAGwDS2BUTvWFHUxPEwT1M_kFxbHbDGGM130_provenance.