Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_assertion description "[L1CAM mutation in a boy with hydrocephalus and duplex kidneys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_assertion evidence source_evidence_literature NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_assertion SIO_000772 17294222 NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_assertion wasDerivedFrom befree-20150227 NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_assertion wasGeneratedBy ECO_0000203 NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP529887.RAKvC1z3GueKnRyi6zEJHdpJzVKr0AfPtBIfXpn_cdjQc130_provenance.