Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_assertion description "[Combined deficiency of factor V (FV) and FVIII (F5F8D) is an autosomal recessive bleeding disorder characterized by simultaneous decreases of both coagulation factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_assertion evidence source_evidence_literature NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_assertion SIO_000772 23852824 NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_assertion wasDerivedFrom befree-2016 NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_assertion wasGeneratedBy ECO_0000203 NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1093797.RApEpV0uykcX7qlKr__fPuVn--k2iLFfOsbvtJGhhPCGI130_provenance.