Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_assertion description "[The use of SNPs in MCC testing allows for precise identification of chromosomal abnormalities in miscarriage as well as MCC, improving the accuracy of products of conception testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_assertion evidence source_evidence_literature NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_assertion SIO_000772 24182409 NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_assertion wasDerivedFrom befree-20140225 NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_assertion wasGeneratedBy ECO_0000203 NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP744372.RA7uhcbBvwcaqT4wDdecFl9TRg1u0-pRjiQHTKY3MRdaI130_provenance.