Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_assertion wasGeneratedBy ECO_0000203 NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_assertion wasDerivedFrom gad-20130706 NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_assertion SIO_000772 20663923 NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_assertion evidence source_evidence_literature NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_assertion description "[A genome-wide scan for common alleles affecting risk for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.
- gad-20130706 importedOn "2013-07-06" NP85095.RAI5pTWZG1P_FhThFlRtv56_uUNfGdQEHE7j3Jqp1fR6c130_provenance.