Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- befree-2016 importedOn "2016-02-19" NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_assertion wasGeneratedBy ECO_0000203 NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_assertion wasDerivedFrom befree-2016 NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_assertion SIO_000772 8972002 NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_assertion evidence source_evidence_literature NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.
- NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_assertion description "[Cosegregation of the protein C gene mutation with protein C deficiency could be determined in 13 families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1364606.RArO46XiZaVv594sG8sHf7jPedyN_sHCATLcHXiGsyXws130_provenance.