Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_assertion description "[The expressed constructs include the intact integrin and two mutants, namely hbeta3(Y747F/Y759F) and hbeta3(S752P), each of which induces the bleeding dyscrasia, Glanzmann's thrombasthenia, in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_assertion evidence source_evidence_literature NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_assertion SIO_000772 16294265 NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_assertion wasDerivedFrom befree-20150227 NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_assertion wasGeneratedBy ECO_0000203 NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP885759.RAy0s7UldxApxAiz1L43LqfStK0QIE2Y8tNVrVHNjfZ7I130_provenance.