Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_assertion description "[Glanzmann thrombasthenia (GT) is caused by a defect in either glycoprotein (GP)IIb (alphaIIb) or GPIIIa (beta3) genes and therefore screening of both genes is required for mutation identification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_assertion evidence source_evidence_literature NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_assertion SIO_000772 9493569 NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_assertion wasDerivedFrom befree-2016 NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_assertion wasGeneratedBy ECO_0000203 NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1390068.RAIYhsfKzvd0Az--XrJwdi_8g6N8Sr3Zs6FXkURQ4pPqY130_provenance.