Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_assertion wasGeneratedBy ECO_0000203 NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_assertion wasDerivedFrom befree-2016 NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_assertion SIO_000772 9615224 NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_assertion evidence source_evidence_literature NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
- NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.