Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_assertion description "[Interestingly, one patient with terminal deletion between 5p15.31-pter lacks mental retardation and cat-like crying, indicating that this region might not be responsible for those cardinal features of 5p- syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_assertion evidence source_evidence_literature NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_assertion SIO_000772 15602631 NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_assertion wasDerivedFrom befree-20140225 NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_assertion wasGeneratedBy ECO_0000203 NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP927139.RAtwexCNRCSfY1havtaEUVaV17nq99V_IjVldTT3ek2bg130_provenance.