Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_assertion description "[Our study thus implies that the Pro56Ser mutation might lead to ALS by eliminating the native MSP structure, which consequently leads to aggregation and loss of functions under physiological conditions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_assertion evidence source_evidence_literature NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_assertion SIO_000772 20377183 NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_assertion wasDerivedFrom befree-20140225 NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_assertion wasGeneratedBy ECO_0000203 NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP654471.RA1qlgz2q3AZmotEE5AjhxwWMN3O_XYU7-vhmB4ut_7Fw130_provenance.