Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_assertion description "[Mutations in the ATP1A2 gene have been described in families with familial hemiplegic migraine (FHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_assertion evidence source_evidence_literature NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_assertion SIO_000772 18028407 NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_assertion wasDerivedFrom befree-2016 NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_assertion wasGeneratedBy ECO_0000203 NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.
- befree-2016 importedOn "2016-02-19" NP641457.RAGkkKqYfzxsG2bpkYJEyCsHRTYpz-3N-7dI9Tb3jfMPU130_provenance.