Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_assertion description "[We studied 16 patients with severe hemophilia A (factor VIII and factor VIII:Ag <1%) with intron 22 inversions of the factor VIII gene and 6 patients with hemophilia B, 2 each having a common mutation, for the common prothrombotic markers in the anticoagulant and fibrinolytic cascade.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_assertion evidence source_evidence_literature NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_assertion SIO_000772 18550475 NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_assertion wasDerivedFrom befree-20150227 NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_assertion wasGeneratedBy ECO_0000203 NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392635.RAQM9bLcTLDvthpYokbBgiUrtHw74abeuBgIDiZDSWgNQ130_provenance.