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- source_evidence_literature type ECO_0000212 NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_assertion description "[A missense mutation (Asn 217 to Ser), which may interfere with calcium binding, was also detected in exon VIII in a patient with type III protein S deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_assertion evidence source_evidence_literature NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_assertion SIO_000772 7545463 NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_assertion wasDerivedFrom befree-20150227 NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_assertion wasGeneratedBy ECO_0000203 NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323093.RAbsj_piilSJaS0LHuNFNpbMG_sjHEx4vRcqcEsUpxBdE130_provenance.