Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_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." NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion evidence source_evidence_literature NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion SIO_000772 20572111 NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion wasDerivedFrom befree-20150227 NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion wasGeneratedBy ECO_0000203 NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance.