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- source_evidence_literature type ECO_0000212 NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_assertion description "[While TPM2 mutations identified so far in muscular diseases were all associated with a dominant inheritance pattern, we report the identification of a homozygous null allele mutation in the TPM2 gene in a patient who presented with a recessive form of nemaline myopathy associated with a non-lethal multiple pterygium syndrome (Escobar-MPS MIM# 265000).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_assertion evidence source_evidence_literature NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_assertion SIO_000772 19155175 NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_assertion wasDerivedFrom befree-2016 NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_assertion wasGeneratedBy ECO_0000203 NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.
- befree-2016 importedOn "2016-02-19" NP715451.RAmfcIIN7NFrHa7pIUbG2bOgy6-EUsw3nx3UN7BB1gJOg130_provenance.