Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_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." NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_assertion evidence source_evidence_literature NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_assertion SIO_000772 17294222 NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_assertion wasDerivedFrom befree-20140225 NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_assertion wasGeneratedBy ECO_0000203 NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP548691.RA0fJqnGvfqnz8zul6H5Xp2argLayCQSsNefAR8cvH40g130_provenance.