Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_assertion description "[The novel mutations identified in this study expand the genetic spectrum of late-onset Pompe disease, and the prevalence of respiratory dysfunction highlights the importance of monitoring pulmonary function in late-onset Pompe patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_assertion evidence source_evidence_literature NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_assertion SIO_000772 25526786 NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_assertion wasDerivedFrom befree-2016 NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_assertion wasGeneratedBy ECO_0000203 NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249810.RAnhw863hKc8VqB0HPLl_ySqDkbIvkccN2vARMmVRO4hc130_provenance.