Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion evidence source_evidence_literature NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion SIO_000772 23609221 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion wasDerivedFrom befree-20150227 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_assertion wasGeneratedBy ECO_0000203 NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357068.RAxl0Wup5nEi0gRRPMf4605mE3jq_jIWrj_WZvMv-QJkY130_provenance.