Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_assertion evidence source_evidence_literature NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_assertion SIO_000772 18723471 NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_assertion wasDerivedFrom gad-20130706 NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_assertion wasGeneratedBy ECO_0000203 NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- gad-20130706 importedOn "2013-07-06" NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.