Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion wasGeneratedBy ECO_0000203 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion wasDerivedFrom befree-20140225 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion SIO_000772 16533976 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion evidence source_evidence_literature NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion description "[Classic Fabry disease, an X-linked recessive lysosomal storage disease due to the deficient activity of alpha-galactosidase A, typically presents in early childhood with acroparesthesias, angiokeratomas, hypohidrosis, and corneal dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.