Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_assertion description "[No functionally significant mutation was identified, suggesting that APXL is not directly involved in OA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_assertion evidence source_evidence_literature NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_assertion SIO_000772 7795590 NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_assertion wasDerivedFrom befree-2016 NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_assertion wasGeneratedBy ECO_0000203 NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1322108.RAHWl5nQ0mNoWFTgZI8rHYZ_cvwML4kpSEmZKZ_Xad4SI130_provenance.