Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_assertion description "[Additional conditions which predispose to neonatal jaundice in the presence of Gilbert's Syndrome, include Coombs' negative ABO blood group heterospecificity, hereditary spherocytosis, and prolonged breastfeeding.Gilbert's Syndrome and G-6-PD deficiency are both common, inherited conditions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_assertion evidence source_evidence_literature NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_assertion SIO_000772 11803413 NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_assertion wasDerivedFrom befree-20140225 NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_assertion wasGeneratedBy ECO_0000203 NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505389.RAiUwXsb9ceEVXQ0EGv6l1QX76ECmqBglDbQjWnUc_m8U130_provenance.