Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion wasGeneratedBy ECO_0000203 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion wasDerivedFrom befree-20140225 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion SIO_000772 10561721 NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion evidence source_evidence_literature NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_assertion description "[The mutations in the helix initiation motif of K13 are the cause of WSN in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP365516.RA8GF2WXF-m238YFZReCwvQzzFXQKK6wXvFUcpS30Bv1M130_provenance.