Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_assertion description "[Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_assertion evidence source_evidence_curated NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_assertion SIO_000772 21129722 NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_assertion wasDerivedFrom uniprot-20150221 NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_assertion wasGeneratedBy ECO_0000218 NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3445.RAcF2YG1XvFKriLLVb191E68t16lb362hd0IOC7CQbXdc130_provenance.