Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_assertion description "[Mutations in the KAL gene (Kallmann syndrome) and the AHC gene (adrenal hypoplasia congenita/HH) cause X-linked recessive HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_assertion evidence source_evidence_literature NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_assertion SIO_000772 10727999 NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_assertion wasDerivedFrom befree-20150227 NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_assertion wasGeneratedBy ECO_0000203 NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP520889.RAPrF8gxLt1OSbRNoog4F4Bro8VM288Wxto3w2KSuEeyo130_provenance.