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- source_evidence_literature type ECO_0000212 NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_assertion description "[The PLN -42 C>G mutation is associated with a benign form of apical hypertrophic cardiomyopathy in this family, though the presence of a healthy adult carrier suggests that other genetic and environmental factors could be involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_assertion evidence source_evidence_literature NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_assertion SIO_000772 16829191 NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_assertion wasDerivedFrom befree-20140225 NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_assertion wasGeneratedBy ECO_0000203 NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP691312.RAxN08d6r6U0gDbYYqgw0t_Z3KzPs8hfNcev9r4sHXA_8130_provenance.