Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_assertion wasGeneratedBy ECO_0000203 NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_assertion wasDerivedFrom befree-20140225 NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_assertion SIO_000772 19592504 NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_assertion evidence source_evidence_literature NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_assertion description "[MDR analysis for intragenic mutations of FOXL2 gene reported in previous BPES studies indicated that the mutations which led to much stronger disturbance of amino acid sequence were responsible for more type I BPES, while other kinds of mutation were responsible for more type II BPES.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833580.RAO5zfKiREGbv2r9MDHVHhZY1ky0lPpWqF_WmLG3Qy_K8130_provenance.