Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_assertion description "[In addition, loss of Fgfr2-IIIb is associated with ventricular anomalies including a thin myocardial wall, abnormal trabeculation and muscular ventricular septal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_assertion evidence source_evidence_literature NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_assertion SIO_000772 16687131 NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_assertion wasDerivedFrom befree-2016 NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_assertion wasGeneratedBy ECO_0000203 NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.
- befree-2016 importedOn "2016-02-19" NP549089.RA2q8hRTclYoCpnXayPoOCGAHt1QyKo4jOLx7I0wc2h94130_provenance.