Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_assertion description "[RAD (21,18,13) for all + RAD (X,Y) for cases with ultrasound abnormalities consistent with Turner syndrome + karyotyping for cases with ultrasound abnormalities seemed to be the best approach for the detection of chromosomal abnormalities when invasive prenatal testing is performed for diagnosis of thalassaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_assertion evidence source_evidence_literature NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_assertion SIO_000772 16421217 NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_assertion wasDerivedFrom befree-20150227 NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_assertion wasGeneratedBy ECO_0000203 NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663442.RAwWoB2pNnT70n2NH2x2P1CZ-07W_4-KRJ_yA30N2UyeQ130_provenance.