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- source_evidence_literature type ECO_0000212 NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_assertion description "[Androgen insensitivity syndrome (AIS) is an X-linked genetic disorder of male sexual differentiation caused by mutations in the androgen receptor (AR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_assertion evidence source_evidence_literature NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_assertion SIO_000772 11587068 NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_assertion wasDerivedFrom befree-20150227 NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_assertion wasGeneratedBy ECO_0000203 NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP250078.RAiv3y_Hr261UBh-fTd6Ck03FKvxn9KwSquFw9F6L6lIg130_provenance.