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- source_evidence_literature type ECO_0000212 NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_assertion description "[Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_assertion evidence source_evidence_literature NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_assertion SIO_000772 19154522 NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_assertion wasDerivedFrom befree-2016 NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_assertion wasGeneratedBy ECO_0000203 NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.
- befree-2016 importedOn "2016-02-19" NP715390.RA7lItV-AhHMtJEn0GbqD1OBL7hOWpV7HfBztvejxEGow130_provenance.