Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_assertion description "[Novel indications for PGD not readily applicable by traditional prenatal genetic diagnosis include avoiding clinical pregnancy termination, performing preconceptional diagnosis (polar body I), obtaining prenatal diagnosis without disclosure of prenatal genotype (nondisclosure), diagnosing adult-onset disorders particularly cancer, and identifying HLA compatible embryos suitable for recovering umbilical cord blood stem cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_assertion evidence source_evidence_literature NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_assertion SIO_000772 20572111 NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_assertion wasDerivedFrom befree-20150227 NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_assertion wasGeneratedBy ECO_0000203 NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882528.RAFGpS9mlGOIifiRmxthz3zFe4NZ4b6m_4UOybj8_cEnI130_provenance.