Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_assertion description "[We previously observed an excessive production of deletions at the HPRT locus in FA lymphoblasts belonging to the relatively rare complementation group D(1) and an increased frequency of glycophorin A (GPA) variants in erythrocytes derived from FA patients (2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_assertion evidence source_evidence_literature NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_assertion SIO_000772 10635999 NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_assertion wasDerivedFrom befree-20140225 NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_assertion wasGeneratedBy ECO_0000203 NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807809.RAhmGoWlHu3_CLaSfRvrgFrPw-1F0GALr2DXwnCApeEZk130_provenance.