Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_assertion description "[To determine the incidence of chromosomal abnormality in sonographically normal fetuses after amniocentesis for elevated maternal serum alpha-fetoprotein (MSAFP), and to compare the spectrum of abnormality with that seen in women undergoing amniocentesis for advanced maternal age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_assertion evidence source_evidence_literature NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_assertion SIO_000772 7539525 NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_assertion wasDerivedFrom befree-20140225 NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_assertion wasGeneratedBy ECO_0000203 NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP501146.RA-cPYeJGCZywqquNS0l5ZO94Adcwwdg2ICT1_ifKi6l0130_provenance.