Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_assertion evidence source_evidence_literature NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_assertion SIO_000772 24319099 NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_assertion wasDerivedFrom befree-20150227 NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_assertion wasGeneratedBy ECO_0000203 NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.