Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_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." NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_assertion evidence source_evidence_literature NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_assertion SIO_000772 22374170 NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_assertion wasDerivedFrom befree-20140225 NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_assertion wasGeneratedBy ECO_0000203 NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP905337.RAlfaeYjT3F34jXrUFc1ActWZSK3ehLMAXJSt3a0MMS7I130_provenance.