Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_assertion description "[The abnormalities in CS are associated with mutations in the CSA or CSB genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_assertion evidence source_evidence_literature NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_assertion SIO_000772 10739753 NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_assertion wasDerivedFrom befree-2016 NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_assertion wasGeneratedBy ECO_0000203 NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.
- befree-2016 importedOn "2016-02-19" NP279510.RAhcezU8jiTXWY-L2L6U-hKi1sirRvTcJdPu6A_x0q_50130_provenance.