Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_assertion description "[Moreover, a low amount of maternal cell contamination in the fetus specimen for the prenatal diagnosis of hemoglobin Barts hydrops fetalis as well as the rare multiplicated ?-globin genes can be identified using this method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_assertion evidence source_evidence_literature NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_assertion SIO_000772 22374170 NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_assertion wasDerivedFrom befree-2016 NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_assertion wasGeneratedBy ECO_0000203 NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP964156.RA1dw7ep_9oDOLjRMwALkd0XzBisZTELb0t3ihrSG8DzQ130_provenance.