Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_assertion description "[In this study the proportion of sporadic and familial malignant melanoma (MM) cases harbouring 1100delC in CHK2 was determined to assess whether this mutation is associated with the occurrence of MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_assertion evidence source_evidence_literature NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_assertion SIO_000772 15057041 NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_assertion wasDerivedFrom befree-20140225 NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_assertion wasGeneratedBy ECO_0000203 NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201363.RAWohKV4R_2rcChty1DDiI07l7k8xw61fZ8HJbFjgqolg130_provenance.