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- source_evidence_literature type ECO_0000212 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion description "[Two genes have been identified for the X-linked forms (dystrophin and tafazzin), while mutations in multiple genes cause autosomal dominant DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion evidence source_evidence_literature NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion SIO_000772 14567970 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion wasDerivedFrom befree-2016 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_assertion wasGeneratedBy ECO_0000203 NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.
- befree-2016 importedOn "2016-02-19" NP417484.RApP36CMi1b_7cD2hsQ12XJs76uwmYOjrvrkWAGYGtZSw130_provenance.