Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_assertion description "[Array-CGH analysis of the patient blood revealed a constitutive 1.4 million base pair deletion at 7q11.23, compatible with WS diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_assertion evidence source_evidence_literature NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_assertion SIO_000772 24753445 NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_assertion wasDerivedFrom befree-20150227 NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_assertion wasGeneratedBy ECO_0000203 NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470459.RAxZnQixdRQ8xHjFBXNadjoX0yh15nPZxQv6u3CqVMZLQ130_provenance.