Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion evidence source_evidence_literature NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion SIO_000772 10852374 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion wasDerivedFrom befree-20150227 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_assertion wasGeneratedBy ECO_0000203 NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP693365.RALKisGD4wO7hfWFP1Gm_6xK0oQ5x05gcMlT5jEniwJ7E130_provenance.