Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_assertion description "[A child with macrocephaly: case report of a patient with megalencephalic leukoencephalopathy with subcortical cysts and a compound heterozygosity for two mutations in the MLC1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_assertion evidence source_evidence_literature NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_assertion SIO_000772 21487377 NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_assertion wasDerivedFrom befree-2016 NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_assertion wasGeneratedBy ECO_0000203 NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.
- befree-2016 importedOn "2016-02-19" NP886621.RA8pI6kW2CPhoR_zwrOPCwYalYFmm5cjkzRgzqxssNtNU130_provenance.