Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_assertion description "[L1CAM mutation in a boy with hydrocephalus and duplex kidneys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_assertion evidence source_evidence_literature NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_assertion SIO_000772 17294222 NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_assertion wasDerivedFrom befree-20140225 NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_assertion wasGeneratedBy ECO_0000203 NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP863897.RAXl7oxJ-38T0-sY2cM2052MJcYrOOKjfh2zullP6IECs130_provenance.