Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_assertion wasGeneratedBy ECO_0000203 NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_assertion wasDerivedFrom befree-20150227 NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_assertion SIO_000772 19507653 NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_assertion evidence source_evidence_literature NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.
- NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_assertion description "[Examination established hereditary thrombophilia: the heterozygotic type gene for MTHFR (C677), deletion/insertion polymorphism for PAI-1 (4G/5G) in women and deletion/insertion polymorphism 4G/5G for PAI-1 and heterozygotic genotype DD (190 bp) for angiotensin converting enzyme (ACE) in man.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349875.RA6dt4r0IoK32vnZ67cEeApIbgv_kGOFCaDNe-P8t-Gbs130_provenance.