Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_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." NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_assertion evidence source_evidence_literature NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_assertion SIO_000772 10727999 NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_assertion wasDerivedFrom befree-20140225 NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_assertion wasGeneratedBy ECO_0000203 NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP384445.RAmqd84oeMbCKT9YCvr1A2yC3_0YN5sXcO98d90j2qjlw130_provenance.