Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_assertion wasGeneratedBy ECO_0000203 NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_assertion wasDerivedFrom befree-20140225 NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_assertion SIO_000772 18285834 NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_assertion evidence source_evidence_literature NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_assertion description "[Putative loss-of-function mutations in PROKR2 or PROK2, encoding prokineticin receptor-2 (a G protein-coupled receptor), and one of its ligands, prokineticin-2, respectively, have recently been reported in approximately 10% of Kallmann syndrome affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682923.RAyMGNcwgdYLUFd7myM_bj0wrvfgqoZW_zwtzAAxekjlw130_provenance.