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- source_evidence_literature type ECO_0000212 NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_assertion description "[Although the frequency of the mutations is low in our series (4 of 188 patients [2%]), our results, similar to those already reported, support a direct pathogenic role of p62 in different types of FTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_assertion evidence source_evidence_literature NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_assertion SIO_000772 24042580 NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_assertion wasDerivedFrom befree-20150227 NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_assertion wasGeneratedBy ECO_0000203 NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP849768.RA0wg-_fRa0Nnj0aJpe4mcXFZb3P3mJywO3PyvNnbtlR4130_provenance.