Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion description "[ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR) and multiple congenital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion evidence source_evidence_literature NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion SIO_000772 15006694 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion wasDerivedFrom befree-20140225 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion wasGeneratedBy ECO_0000203 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.