Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion description "[DNA sequencing of the nine exons and flanking intronic regions of ACTA2 was performed in 39 MMD patients with no family history for MMD or TAAD and 68 healthy controls of central European descent with custom made primers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion evidence source_evidence_literature NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion SIO_000772 20970362 NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion wasDerivedFrom befree-20140225 NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_assertion wasGeneratedBy ECO_0000203 NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP354388.RA-pHymdMzejW6Ms985IpLKzFAclTWY2zpvJxpq948AQ8130_provenance.