Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_assertion description "[DNA analysis of patients reported eight novel mutations of the FXI gene but neither mutation location nor secretion or not of the variant correlated with the bleeding tendency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_assertion evidence source_evidence_literature NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_assertion SIO_000772 20398070 NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_assertion wasDerivedFrom befree-2016 NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_assertion wasGeneratedBy ECO_0000203 NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.
- befree-2016 importedOn "2016-02-19" NP806518.RAHB5XRMzhrVRDPMB00tsndD7QuJpr1GT5JE3NV57uGKo130_provenance.