Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_assertion description "[Mutations in the ARX gene, at Xp22.3, cause several disorders, including infantile spasms, X-linked lissencephaly with abnormal genitalia (XLAG), callosal agenesis and isolated intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_assertion evidence source_evidence_literature NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_assertion SIO_000772 22585566 NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_assertion wasDerivedFrom befree-2016 NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_assertion wasGeneratedBy ECO_0000203 NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.
- befree-2016 importedOn "2016-02-19" NP982202.RAm5r7qkNjf18R72zKNQLQl-AdddnaRe_4FmWDwvo8YJE130_provenance.