Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_assertion description "[We detected 34 in COL4A5, the gene responsible for X-linked Alport syndrome, and 13 in COL4A3 and COL4A4, the genes responsible for autosomal recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_assertion evidence source_evidence_literature NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_assertion SIO_000772 15954103 NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_assertion wasDerivedFrom befree-2016 NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_assertion wasGeneratedBy ECO_0000203 NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.
- befree-2016 importedOn "2016-02-19" NP499315.RAl2ELWJ6aVZMMddYeWyEYX4V_PHpxWrO6KZHGvWqIE0A130_provenance.