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- source_evidence_literature type ECO_0000212 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion description "[The present family shows absent hypopigmentation in two patients of a white family with a deletion in the OA1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion evidence source_evidence_literature NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion SIO_000772 11520764 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion wasDerivedFrom befree-20150227 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_assertion wasGeneratedBy ECO_0000203 NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1002283.RAQINQEmBWjtcVLODlfVvBy9fit_8-WdAb-1Fw48Jm8Xw130_provenance.