Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_assertion description "[DNA investigation established an interstitial deletion in Xp22.3 involving the Kallmann (KAL) gene, the steroid sulfatase (STS) gene and a putative mental retardation locus (MRX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_assertion evidence source_evidence_literature NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_assertion SIO_000772 9727739 NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_assertion wasDerivedFrom befree-20150227 NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_assertion wasGeneratedBy ECO_0000203 NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP620257.RAQh8Irwb1NHpdusy4DorCeqsQuaQQinnL4KLCZWlfmpY130_provenance.