Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_assertion description "[Deletion 11(p11.2p12) is a rare, yet specific, deletion syndrome involving the EXT2 locus, a gene for parietal foramina, and a mental retardation locus, and therefore can be classified as a contiguous gene deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_assertion evidence source_evidence_literature NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_assertion SIO_000772 8882796 NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_assertion wasDerivedFrom befree-20140225 NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_assertion wasGeneratedBy ECO_0000203 NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697136.RAIHx1mhDZ57gXLn4eohS81fWKlZ-ac6TFpdtHZm1cMjI130_provenance.