Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_assertion wasGeneratedBy ECO_0000203 NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_assertion wasDerivedFrom befree-20140225 NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_assertion SIO_000772 10818214 NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_assertion evidence source_evidence_literature NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_assertion description "[We have recently shown that mutations in oligophrenin-1 (OPHN1) are responsible for non-specific X-linked mental retardation (MRX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP412123.RAGhZXvigiU7jXxdDA3wDVKCXs5aCkm2Yb13DxDf_ttMM130_provenance.